Table 5 Probabilities for the event which each haploid at a particular locus is sequence at least twice
From: Genotyping of human neutrophil antigens (HNA) from whole genome sequencing data
| Coverage | P(X1 > 1∩ X2 > 1) |
|---|---|
| 5 | 92.078% |
| 6 | 96.560% |
| 7 | 98.546% |
| 8 | 99.397% |
| 9 | 99.753% |
| 10 | 99.900% |
| 11 | 99.960% |
| 12 | 99.984% |
| 13 | 99.994% |
| 14 | 99.998% |
| 15 | 99.999% |