Variant Details

Variant: esv2107521

Internal ID

7778633

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:244582923..244582960	hg38	UCSC Ensembl
Outer	chr1:244582712..244583163	hg38	UCSC Ensembl
Inner	chr1:244746225..244746262	hg19	UCSC Ensembl
Outer	chr1:244746014..244746465	hg19	UCSC Ensembl
Inner	chr1:242812848..242812885	hg18	UCSC Ensembl
Outer	chr1:242812637..242813088	hg18	UCSC Ensembl

Cytoband

1q44

Allele length

Assembly	Allele length
hg38	452
hg19	452
hg18	452

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv4776669

Samples

NA18507

Known Genes

C1orf101

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)

esv2107521

Frequency

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