Variant DetailsVariant: esv3622736Internal ID | 6662905 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 4696 | hg19 | 4696 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13737695, essv13737694, essv13737696, essv13737699, essv13737700, essv13737698, essv13737697, essv13737702, essv13737701 | Samples | NA18988, NA19068, NA19000, HG02725, NA18953, HG01915, HG03849, NA19316, HG04198 | Known Genes | ARMC4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622736
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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