Variant Details

Variant: essv4899090

Internal ID

7484722

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr12:2768411..2768510	hg38	UCSC Ensembl
Outer	chr12:2768292..2768647	hg38	UCSC Ensembl
Inner	chr12:2877577..2877676	hg19	UCSC Ensembl
Outer	chr12:2877458..2877813	hg19	UCSC Ensembl
Inner	chr12:2747838..2747937	hg18	UCSC Ensembl
Outer	chr12:2747719..2748074	hg18	UCSC Ensembl

Cytoband

12p13.33

Allele length

Assembly	Allele length
hg38	356
hg19	356
hg18	356

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

esv1983049

Supporting Variants

Samples

NA18507

Known Genes

LOC283440

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)

essv4899090

Frequency

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