A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666893



Internal ID9932998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79679387..79684775hg38UCSC Ensembl
chr11:79390431..79395819hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385389
hg195389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5823615, essv5533696, essv6491344, essv6076966, essv6387412, essv6420581, essv5463871, essv5685784, essv5438374, essv5430691, essv6345496, essv6574043
SamplesNA18504, NA19190, NA19396, NA18908, NA19437, NA19114, NA18856, NA18853, NA19472, NA19429, NA19346, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666893
Frequency
Sample Size1151
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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