Variant DetailsVariant: esv3621491Internal ID | 6661670 | Landmark | | Location Information | | Cytoband | 9q31.3 | Allele length | Assembly | Allele length | hg38 | 1225 | hg19 | 1225 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13602185, essv13602186, essv13602184, essv13602183 | Samples | HG01965, HG01351, HG01113, HG01566 | Known Genes | PTGR1, ZNF483 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3621491
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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