Variant DetailsVariant: esv3614044Internal ID | 6654251 | Landmark | | Location Information | | Cytoband | 7q21.12 | Allele length | Assembly | Allele length | hg38 | 10145 | hg19 | 10145 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv12879851, essv12879856, essv12879853, essv12879854, essv12879852, essv12879855 | Samples | HG03455, HG03168, HG02054, HG03380, NA19031, HG03470 | Known Genes | ADAM22 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3614044
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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