Variant DetailsVariant: esv3638552Internal ID | 6678649 | Landmark | | Location Information | | Cytoband | 16q12.1 | Allele length | Assembly | Allele length | hg38 | 229630 | hg19 | 229630 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv518e214 | Supporting Variants | essv15472409, essv15472410 | Samples | HG02375, HG01841 | Known Genes | ITFG1, PHKB | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3638552
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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