Variant DetailsVariant: esv2677707Internal ID | 9597126 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 126 | hg19 | 126 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5779246, essv6104091, essv6223977, essv5575240, essv5803688, essv5446221, essv6242887, essv6018237, essv5611843, essv6147840, essv5457231, essv5752614, essv6469250, essv5993256, essv6237436, essv5835454, essv6205877 | Samples | HG00096, HG01060, HG01356, HG00143, HG01250, NA19005, NA20589, NA20769, HG01124, HG00149, NA20299, HG00152, HG00254, NA18941, HG00310, NA12006, NA19463 | Known Genes | | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2677707
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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