Variant Details

Variant: esv2283787

Internal ID

7954898

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:192640669..192640730	hg38	UCSC Ensembl
Outer	chr1:192640472..192640927	hg38	UCSC Ensembl
Inner	chr1:192609799..192609860	hg19	UCSC Ensembl
Outer	chr1:192609602..192610057	hg19	UCSC Ensembl
Inner	chr1:190876422..190876483	hg18	UCSC Ensembl
Outer	chr1:190876225..190876680	hg18	UCSC Ensembl

Cytoband

1q31.2

Allele length

Assembly	Allele length
hg38	456
hg19	456
hg18	456

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4967758

Samples

NA18507

Known Genes

RGS13

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)

esv2283787

Frequency

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