A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664436



Internal ID9930541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93286999..93296740hg38UCSC Ensembl
chr11:93020165..93029906hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg389742
hg199742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6387798, essv6459553, essv5804283, essv6517167, essv5668176, essv6095076, essv6026918, essv6300498, essv5771328, essv5640430, essv6470080, essv6336926, essv5867861, essv5666536, essv5528728, essv6537100, essv6584813, essv5866118, essv6199454, essv6135635, essv6328265, essv5670573, essv6244738, essv5949980
SamplesHG00100, HG00737, HG01070, NA19762, HG01177, HG00330, HG00236, HG01048, HG01550, HG00253, NA20505, HG01095, NA20760, HG00740, NA19675, NA19652, NA11881, NA12272, NA20804, NA19679, HG01055, NA20510, NA20826, NA11892
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664436
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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