A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3579884



Internal ID18361396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102713373..102759322hg38UCSC Ensembl
Innerchr11:102584104..102630053hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3845950
hg1945950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9798764
Samples401563TK
Known GenesMMP8
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)esv3579884
Frequency
Sample Size873
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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