A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758265



Internal ID9980342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40901308..41061293hg38UCSC Ensembl
Innerchr11:40922858..41082843hg19UCSC Ensembl
Innerchr11:40879434..41039419hg18UCSC Ensembl
Innerchr11:40879434..41039419hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38159986
hg19159986
hg18159986
hg17159986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759822
Supporting Variantsessv10725
SamplesNA18523
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)esv2758265
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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