A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556079



Internal ID16343488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99438277..99461752hg38UCSC Ensembl
Innerchr11:99309008..99332483hg19UCSC Ensembl
Innerchr11:98814218..98837693hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3823476
hg1923476
hg1823476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2122n54
Supporting Variantsnssv781945
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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