Variant DetailsVariant: esv3585579Internal ID | 6625896 | Landmark | | Location Information | | Cytoband | 1p35.3 | Allele length | Assembly | Allele length | hg38 | 4264 | hg19 | 4264 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv9894735, essv9894731, essv9894732, essv9894736, essv9894733, essv9894730, essv9894729, essv9894734 | Samples | HG04222, HG03667, HG02733, HG02490, HG03750, HG03884, HG04219, HG03838 | Known Genes | PHACTR4 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3585579
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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