A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758283



Internal ID9980360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97031969..97177303hg38UCSC Ensembl
Innerchr11:96902969..97048303hg19UCSC Ensembl
Innerchr11:96408179..96553513hg18UCSC Ensembl
Innerchr11:96408179..96553513hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38145335
hg19145335
hg18145335
hg17145335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759855
Supporting Variantsessv15711, essv23549
SamplesNA06993, NA18912
Known Genes
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)esv2758283
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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