A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1449530



Internal ID16100134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125112706..125271154hg38UCSC Ensembl
Outerchr11:124982602..125141050hg19UCSC Ensembl
Outerchr11:124487812..124646260hg18UCSC Ensembl
Outerchr11:124487812..124646260hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38158449
hg19158449
hg18158449
hg17158449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv832290
Supporting Variants
Samples
Known GenesPKNOX2
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nssv1449530
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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