A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777147



Internal ID15724417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64156974..64275525hg38UCSC Ensembl
Innerchr11:63924446..64042997hg19UCSC Ensembl
Innerchr11:63681022..63799573hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38118552
hg19118552
hg18118552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555184
Supporting Variants
Samples
Known GenesBAD, DNAJC4, FERMT3, FKBP2, MACROD1, NUDT22, PLCB3, PPP1R14B, STIP1, TRPT1, VEGFB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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