A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3579796



Internal ID18707994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88550304..88552536hg38UCSC Ensembl
Innerchr11:88283472..88285704hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382233
hg192233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv401e212
Supporting Variantsessv9798517, essv9798508, essv9798505, essv9798515, essv9798501, essv9798496, essv9798516, essv9798500, essv9798512, essv9798497, essv9798519, essv9798506, essv9798502, essv9798513, essv9798507, essv9798503, essv9798511, essv9798494, essv9798509, essv9798518, essv9798523, essv9798498, essv9798522, essv9798495, essv9798504, essv9798520, essv9798514
Samples401706BJ, 401640WJ, 400101EH, 400468OB, 401460LW, 401582GG, 400893ZE, 400827MM, 400343BD, 401780BB, 402065BG, 401401BA, 400348DK, 401133JG, 400107MJ, 400663MD, 401623SN, 401357MH, 401119DK, 401711WS, 400422PN, 400451kh, 401413RG, 401567BD, 400271SR, 401681MS, 400164SS
Known GenesGRM5
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)esv3579796
Frequency
Sample Size873
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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