Product Details

Assay Reference Genome Location: Chr.1:236394411 on build GRCh38
Cytoband: 1q42.3
Species: Homo sapiens
Variation Type: Copy Number

Additional Information

For this assay, SNP(s) [rs79233817] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Target Gene Details

Entrez Gene ID: 128178
Gene Symbol: EDARADD
Gene Name: EDAR associated death domain
Gene Aliases: ECTD11A, ECTD11B, ED3, EDA3
Location: Chr.1:236394380-236484708 on build GRCh38
Assay Gene Location: Overlaps - Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Location	Protein ID
EDARADD	NM_145861.2			NP_665860.2
	AK290862.1	1	68
	AY028913.1			AAK40287.1
	BC128082.1

Target Copy Number Variation Details

DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv1005877	Chr1:235912335 - 237038508 on Build GRCh38	Gain	MTR MT1HL1 LGALS8-AS1 HEATR1 ERO1B GPR137B NID1 EDARADD LGALS8 ACTN2
esv2763410	Chr1:236334208 - 236735742 on Build GRCh38	Gain	LGALS8-AS1 HEATR1 EDARADD LGALS8 ACTN2
nsv549394	Chr1:235876577 - 236629706 on Build GRCh38	Gain	LYST LGALS8-AS1 HEATR1 ERO1B GPR137B NID1 EDARADD LGALS8
nsv1012436	Chr1:235860657 - 236648100 on Build GRCh38	Loss	LYST LGALS8-AS1 HEATR1 ERO1B GPR137B NID1 EDARADD LGALS8

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