Variant Details

Variant: esv1995711

Internal ID

7666822

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr9:101681700..101682448	hg38	UCSC Ensembl
Outer	chr9:101681501..101682649	hg38	UCSC Ensembl
Inner	chr9:104443982..104444730	hg19	UCSC Ensembl
Outer	chr9:104443783..104444931	hg19	UCSC Ensembl
Inner	chr9:103483803..103484551	hg18	UCSC Ensembl
Outer	chr9:103483604..103484752	hg18	UCSC Ensembl

Cytoband

9q31.1

Allele length

Assembly	Allele length
hg38	1149
hg19	1149
hg18	1149

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4760379

Samples

NA18507

Known Genes

GRIN3A

Method

Sequencing

Analysis

Hierarchical clustering of anomalous readpairs was used to identify groupings of five or more readpairs that had a similar size and position. Read pairs were defined as anomalous if they had high-confidence alignments of each individual read that nevertheless were either incorrectly oriented or implied an insert size of at least 3 standard deviations outside the sample median.

Platform

Not specified

Comments

Reference

Bentley_et_al_2008

Pubmed ID

18987734

Accession Number(s)

esv1995711

Frequency

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