A curated catalogue of human genomic structural variation




Variant Details

Variant: essv22404



Internal ID9620786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89835007..89999719hg38UCSC Ensembl
Innerchr11:89568175..89732887hg19UCSC Ensembl
Innerchr11:89207823..89372535hg18UCSC Ensembl
Innerchr11:89207823..89372535hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38164713
hg19164713
hg18164713
hg17164713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758281
Supporting Variants
SamplesNA10861
Known GenesMIR5692A1, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv22404
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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