A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661679



Internal ID9581098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62528558..62528759hg38UCSC Ensembl
chr11:62296030..62296231hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6159195, essv6063816, essv5642226
SamplesHG01072, HG00328, HG01187
Known GenesAHNAK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661679
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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