A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553083



Internal ID15993806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2299609..2300207hg38UCSC Ensembl
Innerchr11:2320839..2321437hg19UCSC Ensembl
Innerchr11:2277415..2278013hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38599
hg19599
hg18599
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764497, nssv764499, nssv764496, nssv764498
Samples
Known GenesC11orf21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553083
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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