Variant Details

Variant: essv24692

Internal ID

9623327

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:55549600..55744786	hg38	UCSC Ensembl
Inner	chr11:55317076..55512262	hg19	UCSC Ensembl
Inner	chr11:55073652..55268838	hg18	UCSC Ensembl
Inner	chr11:55073652..55268838	hg17	UCSC Ensembl

Cytoband

11q11

Allele length

Assembly	Allele length
hg38	195187
hg19	195187
hg18	195187
hg17	195187

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv2758271

Supporting Variants

Samples

NA11829

Known Genes

OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2

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)

essv24692

Frequency

Sample Size	270
Observed Gain	0
Observed Loss	1
Observed Complex	0
Frequency	n/a