Table 2.
UMN0304 alleles combination | UMN0304 haplotype designation | UMN113 allele combination | UMN113 haplotype designation | INRA189 allele combination | INRA189 haplotype 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.