Variant DetailsVariant: esv2676886 Internal ID | 9596305 | Landmark | | Location Information | | Cytoband | 10q25.1 | Allele length | Assembly | Allele length | hg38 | 1140 | hg19 | 1140 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5697566, essv6242287, essv6225485, essv6351953, essv5637589, essv6030239, essv6594676, essv6459001, essv6319919, essv6582485, essv5511140, essv6537037, essv5874377, essv6093581, essv6084989, essv5489835, essv6400376, essv6065503, essv6501254, essv6212514, essv5943432, essv6005909, essv6506037, essv5903581 | Samples | HG00187, NA20802, HG00367, HG00177, NA20806, NA20769, HG00281, NA20759, NA20775, HG00232, HG00282, NA20809, NA20521, NA20536, NA12718, HG00273, HG00285, HG01113, HG01137, HG00319, HG00256, NA18615, HG00125, HG00377 | Known Genes | ADD3 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2676886
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 24 | Observed Complex | 0 | Frequency | n/a |
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