Variant Details

Variant: nssv549393

Internal ID

15213059

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:143741167..143958691	hg38	UCSC Ensembl
Inner	chr7:143438260..143655784	hg19	UCSC Ensembl
Inner	chr7:143069193..143286717	hg18	UCSC Ensembl
Inner	chr7:142830001..143047525	hg16	UCSC Ensembl

Cytoband

7q35

Allele length

Assembly	Allele length
hg38	217525
hg19	217525
hg18	217525
hg16	217525

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

nsv471645

Supporting Variants

Samples

NA11776

Known Genes

CTAGE6, FAM115A, LOC154761, OR2F2

Method

BAC aCGH

Analysis

Array image analysis and normalization were performed using UCSF Spot and Sproc software (Jain et al. 2002). BACs for which only one of the triplicates printed on the array yielded data, or for which the standard deviation of log2 ratio for the triplicates was 10.2, were removed from final analysis. Furthermore, we discarded BACs that failed to yield data in <20% of cases. For each hybridization experiment, we established a threshold log2 ratio of 2 SDs from the mean of all autosomal clones, and BACs that exceeded this threshold in both independent dye-swap experiments were classified as variant.

Platform

GPL4010

Comments

Reference

Sharp_et_al_2005

Pubmed ID

15918152

Accession Number(s)

nssv549393

Frequency

Sample Size	48
Observed Gain	0
Observed Loss	1
Observed Complex	0
Frequency	n/a