Variant DetailsVariant: esv3643886Internal ID | 6683955 | Landmark | | Location Information | | Cytoband | 19p12 | Allele length | Assembly | Allele length | hg38 | 211912 | hg19 | 211912 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv16008197, essv16008201, essv16008195, essv16008200, essv16008198, essv16008194, essv16008199, essv16008196 | Samples | HG04212, HG03663, NA19457, HG02728, HG03625, HG03838, HG03846, HG01862 | Known Genes | ZNF626, ZNF737 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3643886
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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