A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3579737



Internal ID18361249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70413229..70417245hg38UCSC Ensembl
Innerchr11:70259335..70263351hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg384017
hg194017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9798286
Samples401786WD
Known GenesCTTN
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)esv3579737
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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