A curated catalogue of human genomic structural variation
About the Project
Genome Browser
Downloads
Query Tool
Links
Submissions
Statistics
Contact Us
FAQ
Training Resources
Variant Details
Variant: esv2759873
Internal ID
9635332
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr11:131562907..131879091
hg38
UCSC
Ensembl
Inner
chr11:131432801..131748985
hg19
UCSC
Ensembl
Inner
chr11:130938011..131254195
hg18
UCSC
Ensembl
Inner
chr11:130938011..131254195
hg17
UCSC
Ensembl
Cytoband
11q25
Allele length
Assembly
Allele length
hg38
316185
hg19
316185
hg18
316185
hg17
316185
Variant Type
CNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
esv2758289
Samples
NA19222, NA18603, NA19131, NA06993, NA19238, NA19128, NA19210, NA19205, NA11839, NA11840, NA18856, NA19101, NA19206, NA18913, NA19173, NA19093
Known Genes
NTM
Method
BAC aCGH
Analysis
Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
Platform
Agilent
Comments
Reference
Redon_et_al_2006
Pubmed ID
17122850
Accession Number(s)
esv2759873
Frequency
Sample Size
270
Observed Gain
16
Observed Loss
0
Observed Complex
0
Frequency
n/a
Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage
disclaimer