Variant DetailsVariant: esv2677868Internal ID | 9597287 | Landmark | | Location Information | | Cytoband | 19q13.11 | Allele length | Assembly | Allele length | hg38 | 794 | hg19 | 794 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5436065, essv5720656, essv6046668, essv6238562, essv6454934, essv6052580, essv6034263, essv6363119, essv5871880, essv5902174, essv5958650, essv5711350, essv5814556, essv6023906, essv5929007, essv5900928, essv5559544, essv5666489 | Samples | HG00592, NA19055, NA11829, NA18964, NA18611, HG00427, HG00653, NA18566, NA18536, NA18570, NA19003, HG00476, HG00473, HG00672, HG00614, NA19080, HG00595, HG00593 | Known Genes | WDR88 | 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) | esv2677868
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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