A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17929



Internal ID15837158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60126..99349hg38UCSC Ensembl
Outerchr11:60001..107470hg38UCSC Ensembl
Innerchr11:60126..99349hg19UCSC Ensembl
Outerchr11:60001..107470hg19UCSC Ensembl
Innerchr11:50126..89349hg18UCSC Ensembl
Outerchr11:50001..97470hg18UCSC Ensembl
Innerchr11:50126..89349hg17UCSC Ensembl
Outerchr11:43964..97470hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3847470
hg1947470
hg1847470
hg1753507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8753
Supporting Variants
SamplesNA18572
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv17929
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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