Variant Details

Variant: esv2759098

Internal ID

9981243

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr2:153506565..153664271	hg38	UCSC Ensembl
Inner	chr2:154363078..154520784	hg19	UCSC Ensembl
Inner	chr2:154071324..154229030	hg18	UCSC Ensembl
Inner	chr2:154188586..154346292	hg17	UCSC Ensembl

Cytoband

2q23.3

Allele length

Assembly	Allele length
hg38	157707
hg19	157707
hg18	157707
hg17	157707

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

esv2757838

Samples

NA19141, NA19203, NA18862, NA12814, NA18545, NA12248, NA12865, NA18870, NA12813, NA12812, NA18995, NA12802, NA18547, NA12762, NA12761, NA19137, NA19128, NA19159, NA10839, NA11993, NA18605, NA12003, NA18529, NA10838, NA18981, NA19154, NA18532, NA12264, NA19101, NA12144, NA19160, NA18570, NA11882, NA19206, NA06991, NA12716, NA18952, NA19240, NA12874, NA18594, NA18500, NA18505, NA19129, NA18620

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)

esv2759098

Frequency

Sample Size	270
Observed Gain	31
Observed Loss	13
Observed Complex	0
Frequency	n/a