Table 1.
Genotype distribution of single nucleotide variants
| Sample | Het_ SNV | Hom_ SNV | Novel_ SNV | Het_InDel | Hom_InDel | Novel_InDel |
| G1 | 25 | 22 | 2 | 4 | 0 | 7 |
| G2 | 29 | 11 | 0 | 7 | 0 | 7 |
| G3 | 21 | 9 | 1 | 5 | 0 | 7 |
| G4 | 9 | 14 | 1 | 4 | 0 | 7 |
| G5 | 17 | 12 | 2 | 6 | 0 | 5 |
| G6 | 26 | 15 | 1 | 3 | 0 | 7 |
| G7 | 14 | 24 | 1 | 4 | 0 | 7 |
| G8 | 14 | 11 | 2 | 4 | 0 | 7 |
| G9 | 25 | 21 | 0 | 3 | 0 | 5 |
| G10 | 21 | 9 | 1 | 4 | 0 | 6 |
| G11 | 19 | 25 | 0 | 5 | 1 | 6 |
| G12 | 30 | 12 | 0 | 4 | 0 | 4 |
| G13 | 17 | 14 | 1 | 7 | 0 | 7 |
| G14 | 26 | 12 | 0 | 3 | 0 | 5 |
| G15 | 17 | 14 | 0 | 4 | 0 | 6 |
| G16 | 31 | 11 | 4 | 4 | 0 | 8 |
| G17 | 16 | 19 | 1 | 7 | 0 | 6 |
| G18 | 18 | 24 | 1 | 7 | 0 | 7 |
| G19 | 18 | 22 | 2 | 5 | 0 | 4 |
| G20 | 22 | 13 | 1 | 5 | 0 | 6 |
| G21 | 5 | 17 | 4 | 4 | 0 | 8 |
| G22 | 12 | 11 | 2 | 5 | 0 | 6 |
| G23 | 20 | 26 | 1 | 3 | 1 | 5 |
| G24 | 31 | 14 | 2 | 5 | 0 | 6 |
| G25 | 19 | 13 | 2 | 5 | 0 | 7 |
| G26 | 16 | 20 | 1 | 6 | 0 | 4 |
| G27 | 6 | 16 | 2 | 4 | 0 | 6 |
| G28 | 14 | 24 | 1 | 3 | 0 | 4 |
| G29 | 45 | 8 | 0 | 6 | 0 | 6 |
| G30 | 22 | 13 | 1 | 7 | 0 | 6 |
| G31 | 20 | 23 | 3 | 5 | 0 | 6 |
| G32 | 31 | 15 | 0 | 6 | 0 | 5 |
| G33 | 23 | 13 | 0 | 4 | 0 | 4 |
| G34 | 31 | 7 | 2 | 5 | 0 | 6 |
| G35 | 17 | 13 | 2 | 6 | 0 | 6 |
| G36 | 19 | 10 | 0 | 4 | 0 | 5 |
| G37 | 19 | 25 | 1 | 5 | 1 | 7 |
| G38 | 26 | 20 | 1 | 6 | 0 | 6 |
| G39 | 26 | 13 | 2 | 4 | 0 | 8 |
| G40 | 21 | 10 | 1 | 5 | 0 | 6 |
| G41 | 30 | 12 | 1 | 6 | 0 | 7 |
| G42 | 26 | 17 | 1 | 4 | 0 | 7 |
| G43 | 31 | 14 | 1 | 7 | 0 | 7 |
| G44 | 18 | 13 | 0 | 4 | 0 | 6 |
| G45 | 16 | 21 | 0 | 6 | 0 | 7 |
| G46 | 5 | 17 | 4 | 4 | 0 | 6 |
| G47 | 19 | 25 | 0 | 4 | 1 | 6 |
| G48 | 21 | 9 | 2 | 5 | 0 | 4 |
| G49 | 9 | 14 | 0 | 5 | 0 | 4 |
Het_SNV: Heterozygous genotype SNP (annotation by dbSNP); Hom_SNV: Homozygous genotype SNP (annotation by dbSNP); Novel_SNV: Novel SNV (no annotation by dbSNP); Het_InDel: Heterozygous genotype insertion-deletion (InDel) (annotation by dbSNP); Hom_InDel: Homozygous genotype InDel (annotation by dbSNP); Novel_InDel: Novel InDel (no annotation by dbSNP).