Variant DetailsVariant: esv3639552 Internal ID | 6679644 | Landmark | | Location Information | | Cytoband | 16q24.2 | Allele length | Assembly | Allele length | hg38 | 3544 | hg19 | 3544 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv15566705, essv15566699, essv15566689, essv15566687, essv15566701, essv15566693, essv15566695, essv15566702, essv15566707, essv15566704, essv15566688, essv15566697, essv15566711, essv15566692, essv15566710, essv15566708, essv15566686, essv15566690, essv15566700, essv15566706, essv15566685, essv15566698, essv15566694, essv15566684, essv15566703, essv15566709, essv15566691, essv15566696 | Samples | HG01372, NA11881, HG01530, HG01603, NA07037, HG01438, HG00127, HG00112, NA11918, NA20802, HG00148, HG01680, HG02323, NA12044, NA12282, HG01378, HG00315, NA12761, HG00150, HG01113, HG01705, HG01066, HG00255, HG01139, HG02309, HG03716, HG02315, NA19750 | Known Genes | ZC3H18 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3639552
| Frequency | Sample Size | 2504 | Observed Gain | 0 | Observed Loss | 28 | Observed Complex | 0 | Frequency | n/a |
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