A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553080



Internal ID15993803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2289922..2301432hg38UCSC Ensembl
Innerchr11:2311152..2322662hg19UCSC Ensembl
Innerchr11:2267728..2279238hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3811511
hg1911511
hg1811511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174284
SamplesNINDS_173
Known GenesC11orf21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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