A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3580150



Internal ID18708348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121756748..121764384hg38UCSC Ensembl
Innerchr11:121627456..121635092hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg387637
hg197637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9799004
Samples401302LJ
Known Genes
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)esv3580150
Frequency
Sample Size873
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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