Variant DetailsVariant: esv2666357Internal ID | 9585776 | Landmark | | Location Information | | Cytoband | 11q23.3 | Allele length | Assembly | Allele length | hg38 | 618 | hg19 | 618 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5903375, essv6017258, essv5779586, essv5960178, essv6367111, essv6422783, essv5605249, essv5864958, essv6030756 | Samples | NA18519, HG01134, NA19471, HG00160, HG01149, NA19444, NA19468, HG01082, NA19463 | Known Genes | IFT46 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2666357
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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