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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∩
X
2 > 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%
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