Helligkorsgade, K๘lding, 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 gๅrd, Kolding, DK (built 1595; photo from WikimediaCommons by User:Mahlum, 2006)
 
Lineages and Results of Y-DNA Testing for Haplogroup I2
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)

Haplogroup I is found almost exclusively in Europe where it is represented in about 20% of the population, though subclade I2 is decidedly less common than its sister clade, I1.  It's difficult to generalize about I2 because it contains a number of geographically distinct subgroups.  One group of I2a was initially concentrated in the Balkans and is called "Dinaric" (for a mountain range there, the Dinaric Alps), from which location it dispersed with the retreat of the last ice sheets.  Another group is found around the Baltic and North Sea coastal areas, another in the British Isles, and another in Sardinia and Iberia.  The root clade of I2b is uncommon, with a probable origin from an Iberian glacial refugium from which it spread widely in western Europe.  The main variety of I2b, dubbed "Continental," is most common in northwestern Europe, southern Scandinavia, and Britain.  Another group, "Isles," is almost exclusive to the British Isles, with a concentration in Scotland.

Unlike Haplogroup I1, which is universally 8 at marker DYS455, Haplogroup I2 is usually 11 at this marker (sometimes 10 and rarely 9).

So far, eight members of Danish Demes are some form of Haplogroup I2.
Subclade Most
Downstream
SNP†
D
e
m
e
Surname Earliest Known Patrilineal Ancestor n
I2a2-Dinaric M423 1 JØRGENSEN Jens Jørgen Marious Friis JØRGENSEN (1889-1946) — of Krogsbølle Sogn, Skam Herred, Odense Amt, DK 1
I2b1-Root2 M223* 2 LARSEN Lars Hansen (1751- ) — of Dalby, Krogstrup Sogn, Horns Herred, Frederiksborg Amt, DK 1
I2b1-Continental-1 M223 3 ANDERSEN Jakob Andersen — of Toksværd, Toksværd Sogn, Hammer Herred, Præstø Amt, DK 1
M223* 4 ERIKSEN Jørgen ERIKSEN — of Århus, Århus Sogn, Hasle Herred, Århus Amt, DK 1
M223 5 RASMUSSEN Rasmus Jensen (1824-1888) — of Horsens Sogn, Kær Herred, Aalborg Amt, DK 1
I2b1-Continental-2a M223 6 HAMMER Niels HAMMER — of Viborg Amt, DK 1
M223 7 CHRISTENSEN Nels Peter CHRISTENSEN (1869-1951) — emigrant from Denmark to Michigan 1
M223 8 HANSEN Henrick — of Agernæs, Krogsbølle Sogn, Skam Herred, Odense Amt, DK 1
†Greyed SNPs have merely been deduced; boldfaced SNPs have actually been tested.
*All currently known downstream SNPs have been tested and found negative.
Ken Nordtvedt is the guru researching Hg I subclades (see his Excel spreadsheet; modals below are his).  For a table showing modal haplotypes for Hg I varieties in FamilyTreeDNA marker order, please also see my HTML transcription of Nordtvedt's spreadsheet.  Varieties were determined using Jim Cullen's Haplo-I Subclade Predictor.
Y-DNA Haplogroup I2 SNPs and Subclades
(An equal sign in the ISOGG column means the value is the same as FTDNA.)
Mutations Standard
FTDNA ISOGG
M170 P19 L41 M258 P212 P38 PS76 U179 I =
  M253 I1 =
P215=M438=S31 L68 I2 =
  P37.2 I2a =
  M26 L158 L159.1=S169.1 I2a1 =
  M161 I2a1a I2a1a1
L160 I2a1b I2a1a
M423 L178 I2a2 =
  L69.2(=T)=S163.2   I2a2a
M359=P41.2 I2a2a I2a2a1
L161 I2a2b =
L233 I2a3 =
P217=S23 L181 L35=S150 L37=S153 P214=M436=S33 P216=S30 P218=S32 I2b =
  M223 L34=S151 L36=S152 L59 P219=S24 P220=S119 P221=S120 P222=S118=U250 P223=S117 I2b1 =
  M284 I2b1a =
  L126=S165 L137=S166 I2b1a1 =
M379 I2b1b =
P78 I2b1c =
P95 I2b1d =
L39=S155 L38=S154 L40=S156 L65.1=S159.1 I2b2 =

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.)

I2a2-Dinaric, a.k.a., I-M423-Din
Deme 1
Surname Kit # Ysearch
Code

SNP
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
I2a2-M423-DinS Modal Values 13 24 16 11 14 15 11 13 13 13 11 31 17 8 10 11 11 25 15 19 30 12 14 15 15 10 10 21 21 15 12         11 10 11 8 15 15 7 12 10 8 11 9 12 22 22 16 10 12 12 12 7 10 30 21 13 14 10 13 11 11 12 9 per Nordvedt
I2a2-M423-DinN Modal Values 13 24 16 11 14 15 11 13 13 13 11 31 17 8 10 11 11 25 15 20 32 12 14 15 15 10 10 21 21 15 12         11 10 11 8 15 15 7 12 10 8 11 9 12 22 22 16 10 12 12 12 7 10 30 21 13 14 10 13 11 11 12 9 per Nordvedt
               
JØRGENSEN N52741     13 24 16 10 15 15 11 13 13 12 11 31                                                                                                               Pvt3, Poul Friis2, Jens Jørgen Marious Friis1 JØRGENSEN (1889-1946) — of Krogsbølle Sogn, Skam Herred, Odense Amt, DK
Cullen's predictor gives a 50% chance of being Din-S and 50% of being Din-N.  Upgrading to 25 markers would presumably narrow it down to one or the other.  This individual has no matches in the FTDNA database.  His best matches at Ysearch are a few at 10/12, and his best matches at SMGF are a few at 9/11. 
FTDNA deduces his haplogroup to be I-P37.2 (I2a).  Your project admin recommends deep SNP testing, especially given that his 12-marker haplotype appears to be unique.
   

I2b1-Root2, a.k.a., I-M223-Root2
Deme 2
Surname Kit # Ysearch
Code

SNP
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
I2b1-M223-Root2 Modal Values 14 23 16 11 15 16 11 13 12 13 12 29 15 8 10 11 11 26 15 20 29 11 13 14 15 10 10 19 19 17 18         12 10 12 8 15 16 8 11 10 8 11 9 12 21 22 15 11 12 12 16 9 14 25 22 9 13 12 13 11 12 13 11 per Nordtvedt
                 
LARSEN 82373 F2E6Q M223* 14 23 17 11 15 15 11 13 11 13 12 28 15 8 10 11 11 26 16 20 29 11 13 14 15 11 10 19 19 17 17 17 21 36 37 12 10                                                             Pvt7, Pvt6, Christian LARSEN5, Anders Larsen4, Lars Nielsen3, Niels Larsen2, Lars Hansen1 (1751- ) — of Dalby, Krogstrup Sogn, Horns Herred, Frederiksborg Amt, DK
#82373 has a rare haplotype, with no matches at any level in the FTDNA or Ysearch databases.  Cullen's predictor gives him a 68% probability of being I-M223-Root2.
Our subject has opted for deep SNP testing, with these results:
P19+ M170+ M258+ P38+ M223+ P37.2- M161- M26- M21- M227- M253-  M307- M72- P30-
The first four positive results prove our subject is Haplogroup I.  The fifth positive result proves he is I2b1.  The first three negative results confirm that he is not any form of I2a.  The remaining six negative results confirm that he is not any form of I1.
UPDATE:  Our subject has taken the I2b test bundle at EthnoAncestry, with these results:
S23+ S24+ M223+ M284- M379- P78- P95-
The positive result for S23+ proves he is I2b; the positive results for S24 and M233 prove he is I2b1.  The negative results for M284, M379, P78, and P95 show he is not any known subclade of I2b1 so he is, therefore, root/ancestral I2b1*, a.k.a., I-M223* or I-S23*.
   

I2b1-Continental-1, a.k.a., I-M223-Cont1
Deme 3
Surname Kit # Ysearch
User ID

SNP
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
I2b1-Continental-1 Modal Values 14 23 15 10 15 15 11 13 11 14 12 31 15 8 10 11 11 25 14 20 27 11 14 14 15 11 9 19 21 14 14         12 10 11 8 15 16 8 11 10 8 10 9 12 21 22 15 11 12 12 13 9 13 27 20 11 13 12 12 11 12 12 11 per Nordtvedt
                 
ANDERSEN N22636 383M2 M223 14 23 14 10 15 15 11 13 11 14 12 31 15 8 9 11 11 25 14 20 27 11 14 15 15 11 9 19 21 14 14 17 19 34 37 11 10 11 8 15 16 8 11 10 8 9 9 12 21 22 15 11 12 12 13 9 13 27 20 11 13 13 12 10 12 12 11 Pvt [awaiting lineage] Jakob Andersen1 — of Toksværd, Toksværd Sogn, Hammer Herred, Præstø Amt, DK
Cullen's predictor gives our subject a 100% probability of being I-M223-Cont1.  His haplotype is uncommon.  He has just two 12/12 matches and one near match at 25 markers in the FTDNA database.  At 25 or more markers, his haplotype is unique.
Our subject has opted for deep SNP testing, with these results:
P19+ M170+ M258+ P38+ M223+ P37.2- M161- M26- M21- M227- M253- M307- M72- P30-
The first four positive results prove our subject is Haplogroup I.  The fifth positive result proves he is I2b1.  The first three negative results confirm that he is not any form of I2a.  The remaining six negative results confirm that he is not any form of I1.
   
Deme 4
Surname Kit # Ysearch
Code

Most
Downstream
SNP
Actually
Tested
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
I2b1-M223-Cont1 Modal Values 14 23 15 10 15 15 11 13 11 14 12 32 15 8 10 11 11 25 14 20 27 11 14 14 15 11 9 19 21 14 14         12 10 11 8 15 16 8 11 10 8 10 9 12 21 22 15 11 12 12 13 9 13 27 20 11 13 12 12 10 12 12 11 per Nordtvedt
                 
ERIKSEN 64043 KTZM8 M223* 12 23 15 10 15 16 11 13 11 15 12 32 15 8 10 11 11 25 14 20 27 11 14 15 15 11 9 19 21 14 14 16 19 34 39 12 10 11 8 15 16 8 10 10 8 10 9 12 21 22 15 11 12 13 13 9 12 26 20 12 13 12 12 10 12 12 11 Pvt3, Pvt2, Jørgen1 ERIKSEN of Århus, Århus Sogn, Hasle Herred, Århus Amt, DK
#64043 has a rare haplotype, with no matches at any level in the FTDNA database and only some low level matches at Ysearch and SMGF.  His lack of matches appears to stem from unusual values in Markers 393 and 389i (green table cells).  Cullen's predictor gives him a 100% probability of being I-M223-Continental-1.
Our subject has opted for deep SNP testing, with these results:
P19+ M170+ M258+ P38+ M223+ P37.2- M161- M26- M21- M227- M253-  M307- M72- P30-
The first four positive results prove our subject is Haplogroup I.  The fifth positive result proves he is I2b1.  The first three negative redundantly support that he is not I2a.  The remaining six negative results redundantly support that he is not any form of I1.
UPDATE:  Our subject has taken the I2b test bundle at EthnoAncestry, with these results:
S23+ S24+ M223+ M284- M379- P78- P95-
The positive result for S23+ proves he is I2b; the positive results for S24 and M233 prove he is I2b1.  The negative results for M284, M379, P78, and P95 show he is not any known subclade of I2b1 so he is, therefore, root/ancestral I2b1*, a.k.a., I-M223* or I-S23*.
According to Ken Nordtvedt, DYS572=10 is a defining marker for
a cluster within Continental-1, which also contains an Icelander.
 
Deme 5
Surname Kit # Ysearch
User ID

SNP
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
I2b1-M223-Cont-1 Modal Values 14 23 15 10 15 15 11 13 11 14 12 32 15 8 10 11 11 25 14 20 27 11 14 14 15 11 9 19 21 14 14         12 10 11 8 15 16 8 11 10 8 10 9 12 21 22 15 11 12 12 13 9 13 27 20 11 13 12 12 11 12 12 11 per Nordtvedt
                 
RASMUSSEN N16957     14 23 15 10 15 16 11 13 12 14 12 32 15 8 10 11 11 25 14 20 27 11 14 15 15 11 9 19 21 14 14 17 21 34 41 13 10 11 8 15 16 8 11 10 8 10 10 12 21 22 15 11 12 12 14 9 13 27 20 12 13 12 12 11 12 12 11 Pvt… [awaiting lineage] Rasmus Jensen1 (1824-1888) — of Horsens Sogn, Kær Herred, Aalborg Amt, DK
Cullen's predictor gives an 88% probability of being I-M223-Cont1.
   

I2b1-Continental-2a, a.k.a., I-M223-Cont2a
Deme 6
Surname Kit # Ysearch
User ID

Most
Downstream
SNP
Actually
Tested
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
I2b1-M233-Cont-2a Modal Values 15 23 15 10 15 15 11 13 11 14 12 32 15 8 10 11 11 25 14 20 27 11 14 14 15 11 10 19 21 15 14 12 10 11 8 15 16 8 11 10 8 10 9 12 21 22 15 11 12 12 14 9 14 x 20 11 13 12 12 11 12 12 11 per Nordtvedt
                 
HAMMER N20850 WP8GQ M223 15 23 15 10 15 15 11 13 11 14 12 33 14 8  9 11 11 25 14 20 28 11 14 14 15 11 10 19 21 15 14 17 20 34 38 12 10 11 8 15 16 8 11 11 8 10 9 12 21 22 15 11 12 12 15 9 13 28 21 11 13 12 12 11 12 12 11 Pvt [awaiting lineage] Niels1 HAMMER of Viborg Amt, DK
Cullen's predictor gives a 78% probability that our subject is I-M223-Cont2a.  Despite that fact, he has only a handful of matches at 12 markers and only one near match at 25.  At 25 or more makers, his haplotype remains unique.
Our subject has opted for deep SNP testing, with these results:
P19+ M170+ M258+ P38+ M223+ P37.2- M161- M26- M21- M227- M253-  M307- M72- P30-
The first four positive results prove our subject is Haplogroup I.  The fifth positive result proves he is I2b1.  The first three negative results confirm that he is not any form of I2a.  The remaining six negative results confirm that he is not any form of I1.
   
Deme 7
Surname Kit # Ysearch
Code

Most
Downstream
SNP
Actually
Tested
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
I-M223-Cont2a Modals 15 23 15 10 15 15 11 13 11 14 12 31 15 8 10 11 11 25 14 20 27 11 14 14 15 11 10 19 21 15 14         12 10 11 8 15 16 8 11 10 8 10 9 12 21 22 15 11 12 12 14 9 14 x 20 11 13 12 12 11 12 12 11 per Nordtvedt
                 
CHRISTENSEN N58769 DVKAW   14 23 15 10 15 15 11 13 12 13 12 30 15 8 10 11 11 25 14 20 28 11 14 14 14 11 10 19 21 15 14 18 19 36 40 12 10 11 8 15 16 8 11 10 8  9 9 12 20 21 15 11 12 12 15 9 13 26 20 11 13 12 12 12 12 12 11 Pvt [awaiting lineage] Nels Peter1 CHRISTENSEN (1869-1951) — immigrant from Denmark to Michigan
This individual has a rare haplotype.  In the FTDNA and Ysearch databases, he has a handful of 12/12 matches and a few near matches at 25 markers (all in other surnames), but no matches, full or near, at 37 or 67 markers. 
   
Deme 8
Surname Kit # Ysearch
Code

Most
Downstream
SNP
Actually
Tested
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
I-M223-Cont2a Modals 15 23 15 10 15 15 11 13 11 14 12 31 15 8 10 11 11 25 14 20 27 11 14 14 15 11 10 19 21 15 14         12 10 11 8 15 16 8 11 10 8 10 9 12 21 22 15 11 12 12 14 9 14 x 20 11 13 12 12 11 12 12 11 per Nordtvedt
                 
HANSON 128764     15 22 16 10 15 16 11 13 11 14 12 31 16 8 10 11 11 26 14 21 29 11 13 14 15 11 10 19 21 15 14 18 19 35 38 13 11                                                             Pvt7, Pvt6 HANSON, Hans Z.5, Hans H.4, Hans3 HANSEN, Hans2, Henrick1 — of Agernæs, Krogsbølle Sogn, Skam Herred, Odense Amt, DK
Cullen's predictor shows a 43% probability of being I -M223-Continental-2a. 
   


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 table compiled by FTDNA.
For 25 markers:  21 or less is a non-relative; 22-25, please see this table compiled by FTDNA.
For 37 markers:  31 or less is a non-relative; 32-37, please see this table compiled by FTDNA.
For 67 markers:  57 or less is a non-relative; 58-67, please see this table compiled by FTDNA.
For 111 markers:  100 or less is a non-relative; 101-111, please see this table 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 H๘je, Aalborg Amt, DK (photo from WikimediaCommons by User:Bunnyfrosch, 2007).

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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