Variant DetailsVariant: esv2669809Internal ID | 9589228 | Landmark | | Location Information | | Cytoband | 11q13.4 | Allele length | Assembly | Allele length | hg38 | 940 | hg19 | 940 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6278946, essv5625871, essv6153164, essv5558019, essv5416101, essv5683151, essv5495502, essv6185845, essv5684542, essv6086529, essv6245678, essv6125299, essv6567922, essv6591166, essv6583034, essv6542148, essv5491036 | Samples | NA19377, NA19379, NA18874, NA20340, HG01440, NA18867, NA19347, NA18523, NA19108, NA19835, NA19311, NA19818, NA19398, NA18501, NA19116, NA19213, NA19312 | Known Genes | | 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) | esv2669809
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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