A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553545



Internal ID15994268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12206134..12212181hg38UCSC Ensembl
Innerchr11:12227681..12233728hg19UCSC Ensembl
Innerchr11:12184257..12190304hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg386048
hg196048
hg186048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175076
SamplesHGDP00550
Known GenesMICAL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553545
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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