A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661140



Internal ID9580559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62492495..62497363hg38UCSC Ensembl
chr11:62259967..62264835hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384869
hg194869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6026099, essv6275084, essv5579278
SamplesNA19372, NA19431, NA19452
Known GenesAHNAK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661140
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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