Variant Details

Variant: esv1991993

Internal ID

7663104

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr9:111869480..111869788	hg38	UCSC Ensembl
Outer	chr9:111869294..111869987	hg38	UCSC Ensembl
Inner	chr9:114631760..114632068	hg19	UCSC Ensembl
Outer	chr9:114631574..114632267	hg19	UCSC Ensembl
Inner	chr9:113671581..113671889	hg18	UCSC Ensembl
Outer	chr9:113671395..113672088	hg18	UCSC Ensembl

Cytoband

9q31.3

Allele length

Assembly	Allele length
hg38	694
hg19	694
hg18	694

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4964245

Samples

NA18507

Known Genes

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)

esv1991993

Frequency

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