A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758266



Internal ID9980343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41099096..41312361hg38UCSC Ensembl
Innerchr11:41120646..41333911hg19UCSC Ensembl
Innerchr11:41077222..41290487hg18UCSC Ensembl
Innerchr11:41077222..41290487hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38213266
hg19213266
hg18213266
hg17213266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759823
Supporting Variantsessv6125
SamplesNA18532
Known GenesLRRC4C
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)esv2758266
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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