A curated catalogue of human genomic structural variation




Variant Details

Variant: essv23810



Internal ID9960046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81699742..82119580hg38UCSC Ensembl
Innerchr11:81410784..81830622hg19UCSC Ensembl
Innerchr11:81088432..81508270hg18UCSC Ensembl
Innerchr11:81088432..81508270hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38419839
hg19419839
hg18419839
hg17419839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758278
Supporting Variants
SamplesNA12763
Known GenesMIR4300
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)essv23810
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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