Variant DetailsVariant: esv3622450 Internal ID | 6662620 | Landmark | | Location Information | | Cytoband | 10p13 | Allele length | Assembly | Allele length | hg38 | 4488 | hg19 | 4488 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13704472, essv13704460, essv13704473, essv13704469, essv13704471, essv13704456, essv13704465, essv13704461, essv13704464, essv13704470, essv13704458, essv13704459, essv13704466, essv13704453, essv13704468, essv13704457, essv13704454, essv13704462, essv13704467, essv13704463, essv13704455, essv13704452, essv13704451 | Samples | HG02614, HG03366, HG02589, HG03135, HG03452, HG03578, NA19457, HG02981, HG02573, HG02588, NA18520, HG02968, HG02537, HG03311, HG02568, HG02675, HG03028, HG03240, HG03433, HG02814, NA19117, HG03066, NA18522 | Known Genes | ITGA8 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3622450
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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