Variant DetailsVariant: esv2671745 Internal ID | 9591164 | Landmark | | Location Information | | Cytoband | 19p13.3 | Allele length | Assembly | Allele length | hg38 | 135 | hg19 | 135 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5854797, essv5715448, essv6430670, essv6179571, essv6085071, essv5765449, essv6337366, essv5588307, essv6123854, essv5700658, essv6182268, essv6147536, essv6177811, essv5903846, essv6082765, essv5987760, essv6226827, essv5646708, essv6587740, essv5965738, essv5603565, essv6242165, essv5589598, essv6301489 | Samples | HG01173, HG00249, HG01052, HG00257, HG01389, HG01374, HG00315, HG00271, NA19371, HG01048, HG00326, HG01353, HG01183, HG01187, HG01073, HG00273, NA19114, HG00140, HG01108, HG00256, HG00111, HG00329, HG00342, HG00345 | Known Genes | NFIC | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2671745
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
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