Variant Details

Variant: esv10021

Internal ID

11373940

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:242878992..243017534	hg38	UCSC Ensembl
Inner	chr1:243042294..243180836	hg19	UCSC Ensembl
Inner	chr1:241108917..241247459	hg18	UCSC Ensembl

Cytoband

1q43

Allele length

Assembly	Allele length
hg38	138543
hg19	138543
hg18	138543

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv23865

Supporting Variants

essv62575, essv73069, essv79761, essv38441, essv54546, essv54165, essv56332, essv73592, essv47948, essv46426, essv83815, essv58681, essv37031, essv33959, essv71369, essv44874, essv81938, essv48715, essv35600, essv66899, essv64008, essv33126

Samples

NA18502, NA18861, NA18508, NA19190, NA18916, NA12156, NA12828, NA12489, NA18907, NA07045, NA19114, NA11894, NA15510, NA19099, NA19257, NA19225, NA19108, NA19147, NA07037, NA12749, NA19129, NA12776

Known Genes

Method

Oligo aCGH

Analysis

Segment log2 ratios from each sample. This was done running the GADA algorithm (Pique-Regi et al., 2008) using the options "-M 10 -T 10 -a 2.5". Filter non-CNV segments using intensity thresholds. Merge remaining CNV "calls" within each sample. Adjacent calls of the same direction (gain or loss) are merged if both: the distance between calls is less than 10kb, and the distance between calls is less than 10% of the size of the largest of the two calls.

Platform

Sanger H. Sapiens 42mCGH Array 5781_53 726K v1

Comments

Reference

Conrad_et_al_2009

Pubmed ID

19812545

Accession Number(s)

esv10021

Frequency

Sample Size	40
Observed Gain	0
Observed Loss	22
Observed Complex	0
Frequency	n/a