Deme
14
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| Surname |
Kit
# |
Ysearch
User ID |
SNP
Tests |
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 |
| null439
Cluster 1 Modal Values |
13 |
24 |
14 |
11 |
11 |
14 |
12 |
12 |
0 |
13 |
13 |
29 |
17 |
9 |
9 |
11 |
11 |
25 |
15 |
19 |
29 |
15 |
15 |
16 |
17 |
11 |
11 |
19 |
23 |
16 |
16 |
18 |
17 |
38 |
38 |
12 |
12 |
11 |
9 |
15 |
16 |
8 |
10 |
10 |
8 |
10 |
10 |
12 |
23 |
23 |
15 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
12 |
11 |
13 |
11 |
11 |
13 |
12 |
Modals for Null-439 as of 11 Apr 2007; markers in
red, yellow, or orange are differences from Modal R1b. |
| |
|
|
|
|
|
| STRAUB |
82917 |
|
|
13 |
24 |
14 |
11 |
11 |
14 |
12 |
12 |
0 |
14 |
13 |
30 |
17 |
9 |
9 |
11 |
11 |
25 |
15 |
19 |
30 |
15 |
15 |
16 |
17 |
11 |
11 |
19 |
23 |
16 |
15 |
18 |
17 |
36 |
39 |
12 |
12 |
11 |
9 |
15 |
16 |
8 |
10 |
10 |
8 |
10 |
10 |
12 |
23 |
23 |
15 |
10 |
12 |
12 |
15 |
8 |
12 |
22 |
20 |
13 |
12 |
11 |
13 |
10 |
11 |
13 |
12 |
Pvt4, Pvt3,
Gustav
August2, Charles/Carl1
— immigrant to Philadelphia from Wuerttemberg in 1881 |
| #82917 has a null value at DYS439 (red table cell), meaning the indicator
used to locate the marker has been lost, so no count of STRs could be made.
The change in the indicator is a SNP mutation (S26+ = L1+), and this mutation
defines Haplogroup R-1b1a-2a1a-1a3. The mutation appears to have
arisen about 2500 to 3500 years ago. Note that FTDNA will show a
value of 12 for the marker on the assumption that the modal value is what
the count would most likely be if it could be made. |
| This individual has hundreds of matches at 12-markers, but only a few
near matches at 25 or 37 markers (none in surname STRAUB). At 67
markers, he has no matches with anyone. |
| The null439 condition is sufficiently distinct to warrant its own project,
and your admin recommends joining the
null439
DNA Project. The null439 project web site is an excellent source
of information on what a null439 is and what it means. The null439
project has identified two major clusters of haplotypes, with DYS459b=9
(yellow table cell) being the major difference distinguishing Cluster 1
from Cluster 2. The null439 mutation is found thinly in western Europe,
but is concentrated in the British Isles; Cluster 1 is concentrated in
England and, most notably for our purposes, is also found in southern Germany.
The late Leo Little, former administrator of the null439 project, told
me (in Apr 2007) the three German null439's are surnamed BETTINGER, BLY,
and STINER, and are from the region of the Rhine River Valley and Wuerttemberg. |
| Assuming a modal value of 12 for DYS439, our subject's haplotype becomes
quite common, with many near matches, which is not surprising considering
its resemblance to the modal R1b haplotype. It's the S26+ SNP mutation
that makes this group uncommon. Your project admin recommends taking
an S26+ test to confirm the presence of this mutation. |
|
|
|
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