A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777172



Internal ID15724442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64877647..65003707hg38UCSC Ensembl
Innerchr11:64645119..64771179hg19UCSC Ensembl
Innerchr11:64401695..64527755hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38126061
hg19126061
hg18126061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555208
Supporting Variants
Samples
Known GenesATG2A, BATF2, C11orf85, EHD1, GPHA2, MIR192, MIR194-2, MIR6749, MIR6750, PPP2R5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777172
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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