Variant DetailsVariant: esv3613624Internal ID | 6653833 | Landmark | | Location Information | | Cytoband | 7q11.22 | Allele length | Assembly | Allele length | hg38 | 1939 | hg19 | 1939 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12829566, essv12829563, essv12829565, essv12829564, essv12829568, essv12829567 | Samples | HG00663, HG01867, HG00475, HG00708, NA18548, HG00864 | Known Genes | WBSCR17 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3613624
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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