Variant DetailsVariant: esv3625094Internal ID | 6665246 | Landmark | | Location Information | | Cytoband | 11p15.5 | Allele length | Assembly | Allele length | hg38 | 13521 | hg19 | 13521 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13992183, essv13992182, essv13992181 | Samples | HG00626, HG00596, NA12272 | Known Genes | AP2A2, MUC6 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3625094
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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