A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3578660



Internal ID18360172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43398426..43429377hg38UCSC Ensembl
Innerchr11:43419976..43450927hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3830952
hg1930952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9796894
Samples401838EN
Known GenesTTC17
MethodSNP array
AnalysisWe used four separate algorithms to detect CNVs; Affymetrix Chromosome Analysis Suite (ChAS), iPattern, Nexus and Partek. Our primary analysis was performed based on ChAS CNV calls, which were then supported using the remaining three algorithms to construct a confidence set of CNVs. For all algorithms, we have used 8 probes and >1kb as a base line cutoff for CNV detection.
PlatformAffymetrix CytoScan HD 2.7M array
Comments
ReferenceUddin_et_al_2014
Pubmed ID25503493
Accession Number(s)esv3578660
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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