Variant DetailsVariant: esv3623211Internal ID | 6663379 | Landmark | | Location Information | | Cytoband | 10q11.23 | Allele length | Assembly | Allele length | hg38 | 1661 | hg19 | 1661 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13803083, essv13803086, essv13803087, essv13803084, essv13803081, essv13803080, essv13803082, essv13803085, essv13803079 | Samples | HG04202, HG03836, HG04131, HG03953, HG03743, HG04219, HG03702, HG03642, HG04198 | Known Genes | SGMS1 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3623211
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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