Helligkorsgade, Kølding, DK (built 1589; photo from WikimediaCommons by User:Mahlum, 2006)
Danish Demes
a Regional DNA Project for Danish Americans and Danes around the World
Borches gård, Kolding, DK (built 1595; photo from WikimediaCommons by User:Mahlum, 2006)
 
Lineages and Results of Y-DNA Testing for Haplogroups I1d and I1d1
Y-DNA
Results
Hub		 Y-DNA Haplogroups Represented in the Project
and Their Frequency (n tested at FTDNA + n tested elsewhere)		 mtDNA
Results
Hub		 Project
Home
Page
E
(1)		 F
(1)		 G
(5 + 1)		 I1
(25)		 I1d / I1d1
(12 + 1)		 I2
(11)		 J
(2)		 N
(1)		 Q
(1)		 R1a
(10 + 2)		 R1b
(35 + 2)
Y-DNA Haplogroup I1 SNPs and Subclades
(An equal sign in the ISOGG column means the value is the same as FTDNA.)
Mutations Standard
FTDNA ISOGG
P19 L41 M170 M258 P212 P38 PS76 U179 I =
  M253 L118 L121=S62 L123 L124=S64 L125=S65 L157.1 L186 L187 L75 L80 L81
M307 M307.2=P203.2 M450=S109 P30 P40 S63 S66 S107 S108 S110 S11		 I1 =
  M21 I1a =
M227 I1b =
  M72 I1b1 =
P259=M507 I1c =
L22=S142 I1d =
  P109 I1d1 =
L205 I1d2 =
L287 I1d3 =
  L258 I1d3a =
L300 I1d4 =
L211 I1e =
L338   I1f
P215 I2 =
So far, we have 14 Danish Demes Project members who are Haplogroup I1d and two who are I1d1.
Only the two I1d1's have actually been SNP tested, the rest are merely deduced to be I1d (L22+) based on their haplotypes.
Subclade Shorthand Cluster D
e
m
e		 Surname Earliest Known Patrilineal Ancestor _n_
I1d L22 Norse 1 SØRENSEN Jens SØRENSEN of DK and Cheyenne, Wyoming, USA 1
HANSEN of DK, awaiting lineage 1
2 GLAD Christen GLAD (c1600- ) of Nørre Tranders Sogn, Fleskum Herred, Aalborg Amt, DK 1
3 CHRISTENSEN Mads Frederick Theobald CHRISTENSEN of København, DK, and Utah, USA 1
4 HENDRIKSEN Christian Jessen (c1710s- ) of Våbensted Sogn, Musse Herred, Maribo Amt, DK 1
5 WESTERGARD1 Niels JENSEN (1847-1920) of Børglum Herred, Hjørring Amt, DK 1
6 BENDTSEN Hans Jakob Broe BENDTSEN of Hestlund, Bording Sogn, Hammerum Herred, Ringkøbing Amt, DK 1
7 MADSEN native Dane of Hedensted, Hedensted Sogn, Hattling Herred, Vejle Amt, DK 1
8 NEWMAN2 Hemming Hansen (c1790s- ) of Udby, Stege Sogn, Mønbo Herred, Præstø Amt, DK 1
Norse/
ultraNorse-14		 9 LORENZ Lorenz Asmussen (c1720s- ) of DK 1
10 JENSEN Rasmus Mogensen (c1713-1766) of Vejleby Sogn, Fuglse Herred, Maribo Amt, DK 1
11 PETERSON John PETERSEN (c1836- ) of DK, immigrated to U.S. 1
ultraNorse 12 JACOBSEN Søren Jensen (1763- ) of Harlev, Harlev Sogn, Framlev Herred, Århus Amt, DK 1
13 ANDERSEN Ludvig ANDERSEN of Odense Amt, DK 1
I1d1 P109 ultraNorse-1 14 MORCK Niels MØRCHE of Århus Amt, DK 1
15 DAHL Christian August Albertsen (1757-1821) of Dalby, DK 1
1Name deliberately changed upon immigration to the U.S.A., because JENSEN is so common.
2NYMANN / NYMAND.
To view lineages, please scroll to the right.
To view more of the page without scrolling, temporarily reduce the text size or page size in your browser.
Red labels indicate markers that typically mutate more frequently than those labeled in black.
(Empty cells that are darkened indicate tests not ordered.)
Haplogroup I1d-Norse, a.k.a., I-L22-N
Deme 1
Surname Kit # Ysearch
User ID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9
a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
           
SORENSEN N3667 AM9TG 13 23 14 10 14 14 11 14 11 12 11 28                                                                                                               Pvt3, Pvt2, Jens1 SØRENSEN — DK to Cheyenne, WY
HANSEN N77776 - 13 23 14 10 14 14 11 14 11 12 11 28                                                                                                               Pvt
These individuals have a 12/12 match with the modal haplotype for the Norse variety of Haplogroup I1.  This haplotype is the second most common 9-marker haplotype in Denmark.  They have hundreds of matches in the FTDNA and Ysearch databases.  They will need to upgrade to at least 37 markers to determine whether their relationship is real or coincidental.
Cullen's predictor gave these as the highest probabilities for his variety:
I-L22-N =>36%, I-L22-uN1 =>12%, I-L22-uN2 =>12%, and I-L22-uN2a =>12%.
   
Deme 2
Surname Kit # Ysearch
User ID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9
a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
           
GLAD 48960 27RHW 13 23 14 10 14 14 11 12 11 12 11 28 15 8 9 8 11 24 16 20 29 12 14 15 16 10 10 19 21 14 14 17 20 37 37 12 10                                                             Pvt11, Pvt10, Alma Emmanuel Andersen9 GLAD, Niels Peter Andreasen8, Andreas Andersen7, Anders Andersen6, Anders Andersen5, Anders Jensen4, Jens Andersen3, Anders Christensen2, Christen1 GLAD — of Nørre Tranders Sogn, Fleskum Herred, Aalborg Amt, DK
#48960 has a rare haplotype, with only one match at 12 markers (with a RASMUSSEN), only a near match at 27 markers, and no full or near matches at 37 markers.  Oddly enough, his 9-marker haplotype is the second most common 9-marker haplotype in Denmark.  What must be causing the low level of 12-marker matches is the value of 12 at DYS388 (bright green table cell).  Some experimentation at Ysearch shows that this is, indeed, the case.  If we change DYS388 to 14, he gets over a hundred 12-marker matches; with DYS388=13, he gets nearly a dozen 12-marker matches; and with DYS388=12, he gets just the one 12-marker match already mentioned (searches as of 6/06). 
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-N =>36%, I-M253-T13 =>18%, and I-M253-ND =>14%.
This individual has undergone deep SNP testing at FTDNA:
M170+ M258+ P19+ P38+ M253+ M307+ P30+ M21- M227- M72- P37.2- M26- M161- M223-
The first set of positive results support that he is Haplogroup I; the second set of positive results support that he is I1.  The first set of negative results rule out his belonging to subclades I1a, I1b, or I1b1; the second set of negative results redundantly rules out forms of I2. Our subject was deep SNP tested before the L22 SNP was discovered.  Your project admin recommends taking the Extended Deep Clade test to pick up L22 and other new SNPs.
   
Deme 3
Surname Kit # Ysearch
Code		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0		 19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 4
6
4
d		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
               
CHRISTENSEN N22750 JF3KG 13 23 14 11 14 14 11 14 11 12 11 28 15 8 9 8 11 22 16 20 28 12 13 15 16 10 10 19 21 15 14 18 20 35 36 12 10 11 8 15 15 8 11 10 8 9 10 12 21 24 16 10 12 12 19 8 12 25 20 13 13 11 12 10 11 12 11 Pvt [awaiting lineage] Mads Frederick Theobald1 CHRISTENSEN — of København, DK, and Utah, USA
This individual transferred in 12 markers from the National Geographic Society's Genographic Project.  He has a couple dozen or so 12-marker matches in the FTDNA and Ysearch databases (all in other surnames).  While he has a few near matches at 25 and 37 markers, he has no full matches above 12 markers and no near matches at 67 markers.
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-Bothnia =>39%, I-L22-N =>25%, I-L22-uN1 =>18%, and I-M253-T13 =>12%.  While it may appear that Bothnian is the most probable variety, geographically, it's not.  But if you look at the next two, combined, they give a 43% probability of being either Norse or ultraNorse, which makes more sense.
#N22750 has undergone deep SNP testing at FTDNA:
M170+ M258+ P19+ P38+ M253+ M307+ P30+ M21- M227- M72- P37.2- M26- M161- M223-
The first set of positive results support that he is Haplogroup I; the second set of positive results support that he is I1.  The first set of negative results rule out his belonging to subclades I1a, I1b, or I1b1; the second set of negative results redundantly rules out forms of I2.  Our subject was deep SNP tested before the L22 SNP was discovered.  Your project admin recommends taking the Extended Deep Clade test to pick up L22 and other new SNPs.
   
Deme 4
Surname Kit # Ysearch
User ID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9
a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
           
HENDRIKSEN 60702 TAEUS 13 24 14 10 14 14 11 14 12 13 11 29 15 8 9 8 11 23 16 20 28 12 14 15 17 10 10 19 21 14 14 17 21 36 37 12 10 11 8 15 15 8 11 10 8 9 10 12 23 23 15 10 12 12 17 8 13 25 20 13 13 11 12 11 11 12 11 Pvt9, Pvt8, Oscar Peter HENDRIKSEN7, Alfred Severin HENRIKSEN6, Christian Henriksen5, Henrik Christiansen4, Christian Henriksen3, Henrik Christiansen2, Christian Jessen1 of Våbensted Sogn, Musse Herred, Maribo Amt, DK
#60702 has a unique haplotype, with no matches in the FTDNA or Ysearch databases, even at 12 markers.
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-N =>50% and I-M253-ND =>33%.
   
Deme 5
Surname Kit # Ysearch
User ID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9
a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N Modal Values 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
           
JENSEN > WESTERGARD N33193   13 23 14 10 14 14 11 14 11 11 11 27                                                                                                               Pvt3, Peter Anton JENSEN-WESTERGAARD2, Niels JENSEN1— of Børglum Herred, Hjørring Amt, DK
#N33193 transferred in from the National Geographic Society's Genographic Project.  The family was originally surnamed JENSEN, but changed its surname on immigration to the United States.  Even at just 12 markers, his haplotype is unique, with no full matches in the FTDNA, Ysearch, or SMGF databases.  He has many 11/12 matches in the SMGF database, mostly in Scandinavian surnames, most of which are a mis-match at DYS389i where a value of 11 is unusual (green table cell).
Cullen's predictor gave this as the highest probability for his variety:  I-L22-N =>34%.
   
Deme 6
Surname Kit # Ysearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0		 19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 4
6
4
d		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
               
BENDTSEN N44499 RX5TM  13 23 14 11 14 14 11 14 11 12 11 28                                                                                                               Pvt2, Hans Jakob Broe1 BENDTSEN — of Hestlund, Bording Sogn, Hammerum Herred, Ringkøbing Amt, DK
This individual transferred in 12 markers from the National Geographic Society's Genographic Project.  He has a couple dozen or so 12-marker matches in the FTDNA and Ysearch databases (all in other surnames), including with the CHRISTENSEN above.  However, this 12-marker haplotype is too common to declare a match at this level, so I strongly urge the BENDTSEN to upgrade his markers to see whether his match to the CHRISTENSEN is maintained or falls away.
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-N =>30%, I-M253-P =>10%, I-L22-Bothnia =>9%, and I-M253-ND =>9%.
   
Deme 7
Surname Kit # YSearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
               
MADSEN N17837 UQBP6 13 24 14 10 14 14 11 14 11 8 11 24                                                                                                               Pvt [awaiting lineage] — of Hedensted, Hedensted Sogn, Hattling Herred, Vejle Amt, DK
This individual has a rare haplotype, with no matches in the FTDNA or Ysearch databases, even when I set the GD to 6 at Ysearch.  He does have many 9/9 and 8/9 matches in the SMGF databases.  A value of 24 at DYS390 is uncommon for a Haplogrou I1, and a value of 8 at DYS389i is so rare that it isn't even a choice on the dropdown list at SMGF, so I could only search there on 11 markers.  Note that any change in DYS389i is reflected in DYS389ii, so his GD (genetic distance) from the modal haplotype for I1-L22-N is only 5, not 9.
Cullen's predictor gave L-22-Norse as the highest probabilities for his variety:  I-L22-N =>44%  I-L22-uN1 =>8%  I-L22-uN2 =>8%  I-L22-uN2a =>8%  I-L22-Bothnia =>7%  I-M253-ND =>7%...
FTDNA has given our subject a free backbone SNP test with the result that he is P19+ and M253+ securely placing him in Haplogroup I1.  Your project admin recommends deep SNP testing, to prove that L-22 is also positive.
Your project admin also recommends upgrading to at least 37 markers, to find out whether the rest of this haplotype is more typical of an L-22+ or whether its other values are as unusual as his value at DYS389i.
   
Deme 8
Surname Kit # Ysearch
User ID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67 Advanced Markers
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9
a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5		 4
6
1		 4
6
2		 A10
|
G
A
T
A		 C4
/
6
3
5		 B
0
7		 4
4
1		 4
4
5		 4
5
2		 4
6
3
I1-M253-AS1313 Modals 13 22 14 10 13 14 11 14 11 12 11 29 15 8 9 8 11 23 16 20 28 12 14 15 16 11       14 13         12 10 11 8 15 15 8 11 10 8 9 9 12 23 25 16 10 12 12 16 8 13 25 20 13 13 11 13 11 11 12 11 12 12       17 11 31   as per Nordtvedt
I1-L22-N Modals 13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 12 13 15 22 11 17 11 31 21 as per Nordtvedt
             
NEWMAN 12656 WMNNU 14 25 14 10 14 14 11 14 11 12 11 29 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14           12 10                                       13     14               11 13 12 22 11 16 11   21 Pvt6, Pvt5, Kristian Jørgensen4 NYMANN, Hans Jørgensen3, Jørgen Hemmingsen2, Hemming Hansen1 — of Udby, Stege Sogn, Mønbo Herred, Præstø Amt, DK
#12656 has been tested at both FTDNA (Markers 1-25) and at SMGF (Sorensen Molecular Genealogy Foundation — for markers tested only by SMGF, please scroll to the right).  He has a rare haplotype with no full or even near matches in the FTDNA, Ysearch, or SMGF databases.
Cullen's predictor gave these as the highest probabilities for his variety:  I-M253-1313 =>31%, I-L22-N =>26%, and I-L22-NuN-14 =>23%.  Your project admin recommends upgrading to 67 markers to get a solid determination, plus deep SNP testing to determine the status for L22 because, despite the slight edge given AS1313 by the predictor, if you total the next two probabilities, together they come up 49% for L22.
     

Haplogroup I1d-Norse/ultraNorse-14, a.k.a., I1-L22-NuN14
Deme 9
Surname Kit # YSearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1-L-22-NuN14 Modals 13 23 14 10 14 15 11 14 11 12 11 29 15 8 9 8 11 23 16 20 28 12 14 14 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 17 8 12 26 20 13 14 11 12 11 11 12 11 as per Nordtvedt
               
LORENZEN 81976   13 23 14 10 11 15 11 14 11 12 11 29                                                                                                               Pvt [awaiting lineage] Asmus Lorentzen2, Lorenz Asmussen1 — of DK
This individual has a rare haplotype, with no matches in the FTDNA database, no matches closer than 10/12 at Ysearch, and no matches closer than 11/12 at SMGF, though many of these are with Danish surnames.  I recommend upgrading to at least 37 markers to see if any of these near matches actually mean anything.
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-NuN-14 =>47%  I-M253-1313 =>20%  I-M253-uN-1315 =>11%...
   
Deme 10
Surname Kit # Ysearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67 RG Markers
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5		 4
6
1		 4
6
2		 A10
|
G
A
T
A		 C4
/
6
3
5		 B
0
7
I1-L22-NuN14 Modals 13 23 14 10 14 15 11 14 11 12 11 29 15 8 9 8 11 23 16 20 28 12 14 14 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 17 8 12 26 20 13 14 11 12 11 11 12 11   13       as per Nordtvedt
               
JENSEN RG-002 BXSZ3 13 23 14 11 11 15 11 14 10 12 11 29       8 11 23 16             10 10 19 21               10                                                             12 13 13 21 12 Pvt7, Julius Peter Daneskjold6, Jens Jørgen JENSEN5, Christen Jensen4, Jens Christensen3, Christen Rasmussen2, Rasmus Mogensen1 — of Vejleby Sogn, Fuglse Herred, Maribo Amt, DK
This individual was tested at Relative Genetics (please scroll to the right to see markers exclusive to RG).  He most closely resembles the Norse/ultraNorse transitional variety of I1, but his value of 11 at DYS385a is unusual.  His haplotype is rare, and he has no matches above 9 markers in either the Ysearch of SMGF databases. 
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-NuN-14 =>35%, I-M253-T2 =>11%, and I-M253-T13 =>11%...
Due to differing laboratory standards, the value of GATA-H4 as tested at RG needs to be reduced by one to be equivalent to the same marker as tested by FTDNA.  Our subject's value at this marker as reported by RG was 11, so I have reduced it to 10 in the row above.
     
Deme 11
Surname Kit # Ysearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1-L22-NuN14 Modal Values 13 23 14 10 14 15 11 14 11 12 11 29 15 8 9 8 11 23 16 20 28 12 14 14 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 17 8 12 26 20 13 14 11 12 11 11 12 11 as per Nordtvedt
             
PETERSON N88193 - 13 24 14 11 14 15 11 14 11 12 11 29                                                                                                               Pvt…
Cullen's predictor gave these as the highest probabilities for his variety: 
   
Haplogroup I1d-ultraNorse-?, a.k.a., I1-L22-uN?
Deme 12
Surname Kit # Ysearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9
a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1-M253-ND Modals 13 23 14 10 14 14 11 14 12 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 15 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 19 13 13 11 12 11 11 12 11 as per Nordtvedt
I1-L22-uN1 Modals 13 23 14 10 14 15 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
           
JACOBSEN 105238   13 23 14 10 14 15 11 14 12 12 11 28                                                                                                               Pvt6, Pvt5, Oscar Marius4 JACOBSEN, Anders Peter Jacobsen3, Jacob Sørensen2, Søren Jensen1 — of Harlev, Harlev Sogn, Framlev Herred, Århus Amt, DK
#105238 has several dozen 12/12 matches outside the project, but none in his surname.  In fact, he has the 4th most common 9-marker haplotype in Denmark.  What keeps him from having many more matchees is the value of 12 at DYS439, which is uncommon (DYS439 is not included in the 9-marker haplotype).  Your project admin recommends upgrading to more markers and uploading results to the Ysearch database to increase the probabilty of making a match.
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-uN1 =>22%, I-L22-uN2 =>22%, I-L22-uN2a =>22%, and I-M253-ND =>21%.  Until our subject upgrades to more markers, it simply won't be possible to place him securely by variety, though he is most likely some variety of ultraNorse.
With regard to this individual's lineage, the mother of Oscar Marius5 married Anders Peter Jacobsen4 after Oscar was born; so one purpose of this testing is to determine whether or not Anders is Oscar's biological father.
   
Deme 13
Surname Kit # YSearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1-M253-ND Modal Values 13 23 14 10 14 14 11 14 12 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 15 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 19 13 13 11 12 11 11 12 11 as per Nordtvedt
I1-L22-uN1 Modal Values 13 23 14 10 14 15 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 as per Nordtvedt
               
ANDERSEN N57487   13 23 14 10 15 15 11 14 12 12 11 28                                                                                                             Pvt3, Pvt2, Ludvig1 — of Odense Amt, DK
This individual has five 12/12 matches in the FTDNA database (and two at Ysearch, who are among the five at FTDNA). 
Cullen's predictor gave these as the highest probabilities for his variety:  I-L22-uN1 =>22%, I-L22-uN2 =>22%, I-L22-uN2a =>22%, and I-M253-ND =>20%.  Until our subject upgrades to more markers, it simply won't be possible to place him securely by variety, though he is most likely some variety of ultraNorse.
   
Haplogroup I1d1-ultraNorse-1, a.k.a., I1-P109
Deme 14
Surname Kit # Ysearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67  
3
9
3		 3
9
0
19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 d
|
4
6
4		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5		 4
6
2
I1-L22-uN1 Modals 13 23 14 10 14 15 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 18 8 13 26 20 13 13 11 12 11 11 12 11 13 as per Nordtvedt
               
MORCK N15923 789C8 13 23 14 10 14 15 11 14 13 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14 17 23 37 38 12 10 11 8 15 15 8 11 11 8 9 10 12 23 25 15 10 12 12 18 8 13 26 20 13 13 11 12 11 11 12 11 13 Pvt12, Pvt11 MORCK, Frederik Dorph10, Frederik Vilhelm Pfaff9, Christian Dreyer8, Christian7, Christian Pedersen6, Peder Pedersen5 MØRCK, Peder Jensen4, Jens Jensen3, Jens Nielsen2, Niels1 MØRCHE — of Århus Amt, DK
This individual is a close match to Nordtvedt's ultraNorse1 variety of Haplogroup I1.  His 9-marker haplotype is the fourth most common 9-marker haplotype in Denmark and is the most common 9-marker ultraNorse haplotype in Denmark.  Even so, in the FTDNA database, he has only four full matches at 12 markers and one full match at 25 markers (all in other surnames), and the reason for having so few matches is the value of DYS439=13.  Nordtvedt indicates that, so far, these five individuals are the only I1-uN's with this value for this marker.  At 37 markers or above, our subject's haplotype remains unique.
This individual has been deep SNP tested, with the result that he is M253+ and P109+ making him I1d1.  (It is presumed he is L22+.)
Our subject has custom tested Marker DYS462, a key marker (in addition to DYS511) separating Nordvedt's Norse/ultraNorse varieties from his AngloSaxon varieties of I1, and his test result confirms he is Norse/ultra-Norse.  (The Norse/ultraNorse varieties are 13 at this marker, while the Anglo-Saxon varieties are 12.)  This marker is part the the SMGF set (Sorensen Molecular Genealogy Foundation), so there is a large database including this marker, which Nordtvedt has thus included in his research.
Our subject has undergone a Kittler test (to determine the true order of markers DYS385ab), with a result of 15-14.  Without a Kittler test, the ordering of the pair is unknown and they are, by convention, listed "lo-hi."  Ken Nordtvedt indicates that, as more I1-uN's become Kittler tested, most are turning up lo-hi, with the exception of I1-uN-1, which is turning up hi-lo.
    There is a potential link to this lineage:
Hans Myrk (1280-1335) of Nørre Jylland — said to have been knighted by King Erik Menved VI in 1311
_Tulle Mørk (1335-1400) of Nagbøl, Ribe
__Tuli Mørk (1360-    ) of Nagbøl, Ribe
___NN Mørk (1390-    ) of Nagbøl, Ribe
____Mads Mørch (1420-    ) of Nagbøl eller Fjaltring
_____Christen Madsen Mørch (1460-1526) of Ørs Hovedgaard
______1.  Mads Christensen Mørch (1490-1551)
______2.  Peder Christensen Mørch (1492-    ) 
______3.  Jens Christensen Mørch (1495-    ) 
______4.  Eske Christensen Mørch (1497-    )
Deme 15
Surname Kit # Ysearch
UserID		 Haplotype — as determined by STR testing Known Lineage
Markers 1-12 Markers 13-25 Markers 26-37 Markers 38-67
3
9
3		 3
9
0		 19
/
3
9
4		 3
9
1		 a
|
3
8
5		 b
|
3
8
5		 4
2
6		 3
8
8		 4
3
9		 i
|
3
8
9		 3
9
2		 ii
|
3
8
9		 4
5
8		 a
|
4
5
9		 b
|
4
5
9		 4
5
5		 4
5
4		 4
4
7		 4
3
7		 4
4
8		 4
4
9		 a
|
4
6
4		 b
|
4
6
4		 c
|
4
6
4		 4
6
4
d		 4
6
0		 H4
|
G
A
T
A		 IIa
|
Y
C
A		 IIb
|
Y
C
A		 4
5
6		 6
0
7		 5
7
6		 5
7
0		 a
|
C
D
Y		 b
|
C
D
Y		 4
4
2		 4
3
8		 5
3
1		 5
7
8		 a
|
S1
3
9
5		 b
|
S1
3
9
5		 5
9
0		 5
3
7		 6
4
1		 4
7
2		 S1
4
0
6		 5
1
1		 4
2
5		 a
|
4
1
3		 b
|
4
1
3		 5
5
7		 5
9
4		 4
3
6		 4
9
0		 5
3
4		 4
5
0		 4
4
4		 4
8
1		 5
2
0		 4
4
6		 6
1
7		 5
6
8		 4
8
7		 5
7
2		 6
4
0		 4
9
2		 5
6
5
I1d-L22-N modals   13 23 14 10 14 14 11 14 11 12 11 28 15 8 9 8 11 23 16 20 28 12 14 15 16 10 10 19 21 14 14         12 10 11 8 15 15 8 11 10 8 9 10 12 23 25 15 10 12 12 16 8 13 25 20 13 13 11 12 11 11 12 11 per Nordtvedt
               
DAHL 173756   13 23 14 10 14 14 11 13 11 12 11 28 15 8 9 8 11 24 16 20 28 12 14 15 16 10 10 19 21 14 14 18 20 35 35 11 10 11 8 15 15 8 11 10 8 9 10 12 23 23 15 10 12 12 17 8 13 25 20 13 13 11 12 11 11 12 11 Pvt8, Pvt7, Harold Edward6, Martinus Jensen5, Jens Christian4, Christian Jensen3 DAHL, Jens Christiansen2 Ansager, Christian August Albertsen1 (1757-1821) of Dalby, DK
- 
Cullen's predictor gave these as the highest probabilities for his variety:
I-L22-N =>53%  I-M253-ML =>14%  I-L22-uN1 =>11%
The I-L22-Norse variety as been changed into Haplogroup I-P109-N by Nordtvedt; the predictor has not been updated to reflect that fact, nor do we have a modal for P109.
Our subject has been deep SNP tested, with these results:
M253+ L22+ P109+ P259- M72- M227- M21- L287- L258- L205-
The positive results prove he is Haplogroup I1d1; the negative results redundantly support that he is. 
   

What constitutes a match?
Matches in other surnames are usually mere coincidence, so please ignore them — I'll let you know when you shouldn't!
For 12 markers:  9 or less is a non-relative; 10-12, please see this Chart compiled by FTDNA.
For 25 markers:  21 or less is a non-relative; 22-25, please see this Chart compiled by FTDNA.
For 37 markers:  31 or less is a non-relative; 32-37, please see this Chart compiled by FTDNA.
For 67 markers:  55 or less is a non-relative; 56-67, please see this Chart compiled by FTDNA.
For any test:  0 matching markers, please contact NASA.

Danish Demes
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Memorial stone for King Erik I (c1060-1103), a.k.a., 'Erik the Good' or Erik Ejegod; Borgvold, Viborg Amt, DK (photo from WikimediaCommons by User:Calvin, 2007). Viking burial ground (700-1150 CE), Lindholm Høje, Aalborg Amt, DK (photo from WikimediaCommons by User:Bunnyfrosch, 2007).

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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