Variant Details

Variant: esv2758897

Internal ID

9981042

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrX:142781914..142980929	hg38	UCSC Ensembl
Inner	chrX:141869700..142068715	hg19	UCSC Ensembl
Inner	chrX:141697366..141896381	hg18	UCSC Ensembl
Inner	chrX:141595220..141794235	hg17	UCSC Ensembl

Cytoband

Xq27.2

Allele length

Assembly	Allele length
hg38	199016
hg19	199016
hg18	199016
hg17	199016

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2758595

Samples

NA18621, NA12814, NA07029, NA12146, NA19098, NA18633, NA12155, NA18967, NA18563, NA19192, NA19171, NA19005, NA18944, NA18995, NA12762, NA12005, NA18970, NA18966, NA19007, NA12752, NA07022, NA18948, NA18503, NA19000, NA12144, NA18608, NA18914, NA18632, NA11881, NA18961, NA18952, NA12874, NA19223, NA19211, NA10860, NA18624, NA18622, NA18965

Known Genes

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)

esv2758897

Frequency

Sample Size	270
Observed Gain	0
Observed Loss	38
Observed Complex	0
Frequency	n/a