Skipped variants not on autosomes: 10
Skipped variants with multi-allelic alt: 529
Skipped variants with low depth: 17099
Skipped variants for which no depth could be determined: 0
Skipped variants with (partially) unknown genotype: 500
Skipped variants with invalid genotype: 0

Variants checked: 29721
Mendelian error rate: 1.15%
