Product Details

Assay Reference Genome Location: Chr.X:14839507 on build GRCh38
Cytoband: Xp22.2
Species: Homo sapiens
Variation Type: Copy Number

Additional Information

For this assay, SNP(s) [rs145109079] 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: 2187
Gene Symbol: FANCB
Gene Name: Fanconi anemia complementation group B
Gene Aliases: FA2, FAAP90, FAAP95, FAB, FACB
Location: Chr.X:14690863-14873255 on build GRCh38
Assay Gene Location: Within Intron 11

Gene Symbol	Transcript Accession	Exon Location	Assay Location	Protein ID
FANCB	XM_011545470.2			XP_011543772.1
FANCB	XM_017029356.1			XP_016884845.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv6812	ChrX:14836320 - 14868456 on Build GRCh38	Deletion	FANCB
nsv9934	ChrX:14730738 - 15173654 on Build GRCh38	Loss	MOSPD2 GLRA2 FANCB

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