|
UMN0304alleles combination
|
UMN0304haplotype designation
|
UMN113allele combination
|
UMN113haplotype designation
|
INRA189allele combination
|
INRA189haplotype designation
|
Haplo-group
|
Freq
|
|---|
|
215-225
|
1
|
131
|
1
|
148-153-158-166
|
2
|
{1,1,2}
|
0,014
|
|
217-227
|
2
|
133
|
2
|
148-153-158-164
|
3
|
{2,2,3}
|
0,110
|
|
205-215-225
|
3
|
131-157
|
4
|
148-162
|
5
|
{3,4,5}
|
0,014
|
|
205-215-225
|
3
|
131-155
|
5
|
148-158
|
5
|
{3,5,5}
|
0,069
|
|
205-215-225
|
3
|
131-155
|
5
|
148-158
|
8
|
{3,5,8}
|
0,027
|
|
205-217
|
4
|
131-159
|
3
|
160
|
6
|
{4,3,6}
|
0,123
|
|
205-217
|
4
|
131-157
|
4
|
160
|
6
|
{4,4,6}
|
0,082
|
|
205-215-223
|
5
|
131-155
|
5
|
148-160
|
7
|
{5,5,7}
|
0,123
|
|
205-215-223
|
5
|
131-155
|
5
|
148-158
|
8
|
{5,5,8}
|
0,014
|
|
205-215-223
|
5
|
131-155
|
5
|
151-156
|
9
|
{5,5,9}
|
0,055
|
|
205-215-223
|
5
|
131-147-155
|
6
|
148-158
|
5
|
{5,6,5}
|
0,027
|
|
205-217-223
|
6
|
131-157
|
4
|
160
|
6
|
{6,4,6}
|
0,014
|
|
205-217-223
|
6
|
131-157
|
4
|
148-160
|
7
|
{6,4,7}
|
0,027
|
|
205-217-223
|
6
|
131-155
|
5
|
148-160
|
7
|
{6,5,7}
|
0,014
|
|
215-223
|
7
|
131-155
|
5
|
148-160
|
7
|
{7,5,7}
|
0,041
|
|
205-215
|
8
|
131-155
|
5
|
148-158
|
8
|
{8,5,8}
|
0,014
|
|
205-217-227
|
9
|
131-155
|
5
|
148-158
|
8
|
{9,5,8}
|
0,014
|
|
217-223
|
10
|
131-133-147-155
|
7
|
137-148-158-162
|
12
|
{10,7,12}
|
0,014
|
|
205-215-227
|
11
|
133-155
|
9
|
148-158
|
8
|
{11,9,8}
|
0,055
|
|
205-221-227
|
12
|
131-155
|
5
|
148-158
|
8
|
{12,5,8}
|
0,027
|
|
205-213-227
|
13
|
131-155
|
5
|
151-156
|
9
|
{13,5,9}
|
0,014
|
|
205-213-227
|
13
|
131-155
|
5
|
151-160
|
1
|
{13,5,1}
|
0,014
|
|
205-213-227
|
13
|
131-155
|
5
|
148-158
|
8
|
{13,5,8}
|
0,014
|
|
217-225-227
|
14
|
131
|
1
|
148-153-158-164
|
3
|
{14,1,3}
|
0,027
|
|
213-225
|
15
|
133-147-155
|
8
|
151-153-162
|
11
|
{15,8,11}
|
0,014
|
|
205-215-223
|
5
|
131-155
|
5
|
148-151
|
10
|
{5,5,10}
|
0,041
|
- Each haplotype was attributed a number to designate the combination of alleles for each of the three loci because they can appear as multicopies on the Y-chromosome. The haplogroup is thus defined as the combination of the haplotypes, written as {n UMN1113 haplotype, n UMN0304 haplotype, n INRA189 haplotype}, where n UMN1113 haplotype = 1,…,15, n UMN0304 haplotype = 1,…,9, and n INRA189 haplotype = 1,…,12.
