A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668494



Internal ID9934599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65299941..65300692hg38UCSC Ensembl
Outerchr11:65299902..65300749hg38UCSC Ensembl
Innerchr11:65067412..65068163hg19UCSC Ensembl
Outerchr11:65067373..65068220hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6155309, essv5936114, essv5753581, essv5586175, essv6047138, essv5527903, essv5895731, essv6452020, essv5794964, essv6419950, essv6149214, essv6414316, essv5747614, essv6346024, essv6361495, essv5781725, essv6191647, essv6204694, essv6086956, essv5530388, essv5762785, essv5454028, essv6152860, essv5629151, essv5582170, essv5538282, essv6213560, essv5873138
SamplesNA12842, HG00536, NA11933, NA18959, NA12750, NA18519, NA18547, NA11930, NA12282, NA11932, HG00427, HG00268, HG00557, NA11919, NA12829, NA18499, NA18856, NA18853, NA18576, NA18608, NA20773, NA18961, NA07051, NA18609, NA19102, NA11892, NA18522, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668494
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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