Variant Details

Variant: esv2335907

Internal ID

7660333

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr19:8449539..8449834	hg38	UCSC Ensembl
Outer	chr19:8449352..8450029	hg38	UCSC Ensembl
Inner	chr19:8514423..8514718	hg19	UCSC Ensembl
Outer	chr19:8514236..8514913	hg19	UCSC Ensembl
Inner	chr19:8420423..8420718	hg18	UCSC Ensembl
Outer	chr19:8420236..8420913	hg18	UCSC Ensembl

Cytoband

19p13.2

Allele length

Assembly	Allele length
hg38	678
hg19	678
hg18	678

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4703084

Samples

NA18507

Known Genes

HNRNPM

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)

esv2335907

Frequency

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