Files | 1 |
Samples | 1 |
Input Variants | 462 |
Reference Mismatches | 0 |
Tree Overlap (%) | 49.02 |
Strand Flips | 0 |
Out Of Range Variants | 0 |
Multiallelic Variants | 0 |
Indel Variants | 5 |
VCF Filtered Variants | 0 |
Duplicate Variants | 0 |
Low Sample Call Rate | 0 |
Monomorphic Variants | 0 |
Variant Call Rate < 90% | 0 |
Sample | Haplogroup | Quality | Ns | Coverage | Range | Mutations |
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