Variant DetailsVariant: esv2656589Internal ID | 9576008 | Landmark | | Location Information | | Cytoband | 11q21 | Allele length | Assembly | Allele length | hg38 | 441 | hg19 | 441 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6544350, essv5706449, essv6232058, essv5508428, essv6323481, essv6230664, essv5839866, essv6572292, essv6327247, essv6245494, essv5796382, essv5910559, essv5918092, essv5672557, essv6033488, essv5945606, essv5842651, essv6582412 | Samples | NA11829, NA20531, NA12045, NA12155, NA07347, NA18520, HG00731, NA20521, HG00263, NA12249, NA18853, HG01204, NA18953, HG00136, NA12763, HG00312, NA12006, NA20754 | Known Genes | PANX1 | 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) | esv2656589
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 18 | Observed Complex | 0 | Frequency | n/a |
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