A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19886



Internal ID15494623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77940535..77956815hg38UCSC Ensembl
Outerchr11:77940086..77981532hg38UCSC Ensembl
Innerchr11:77651581..77667861hg19UCSC Ensembl
Outerchr11:77651132..77692578hg19UCSC Ensembl
Innerchr11:77329229..77345509hg18UCSC Ensembl
Outerchr11:77328780..77370226hg18UCSC Ensembl
Innerchr11:77329229..77345509hg17UCSC Ensembl
Outerchr11:77328780..77370226hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3841447
hg1941447
hg1841447
hg1741447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8841
Supporting Variants
SamplesNA19007
Known GenesINTS4
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)nssv19886
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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