Variant DetailsVariant: esv2660397 Internal ID | 9579816 | Landmark | | Location Information | | Cytoband | 9q31.1 | Allele length | Assembly | Allele length | hg38 | 240 | hg19 | 240 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv5842109, essv5451414, essv5545493, essv5978463, essv6360937, essv5663500, essv6430317, essv6370862, essv6187085, essv6301710, essv6014810, essv5713890, essv6408909, essv5775266, essv6347371, essv5980479, essv5561771, essv6034406, essv6316976, essv5656963, essv5476042, essv6462430, essv6379554, essv5548503, essv6026544, essv5671225, essv5490908, essv6098073, essv5417254, essv6319551, essv5853618, essv6403588, essv6101569, essv5726000, essv6107814, essv5442056, essv5554027, essv6337515 | Samples | HG01441, HG01173, HG00671, NA19704, HG01389, HG01374, HG00315, NA18602, HG01350, HG01366, HG01070, HG00689, HG00281, HG01069, HG01170, HG01072, HG00705, HG00108, HG00653, HG00436, NA18534, HG00619, HG00284, HG00331, HG01334, HG00463, HG00246, HG00258, HG01375, HG00237, HG00707, HG00513, HG00259, HG00252, HG01082, HG01061, HG00581, NA18620 | Known Genes | CYLC2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660397
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 38 | Observed Complex | 0 | Frequency | n/a |
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