Hs03530257_cn

• Gene Symbol: C4orf51
• Assay Reference Genome Location: Chr.4:145686882 on build GRCh38
• Cytoband: 4q31.21

Target Gene Details

• Entrez Gene ID: 646603
• Gene Name: chromosome 4 open reading frame 51
• Gene Aliases: -
• Location: Chr.4:145680103-145792248 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
C4orf51	NM_001080531.1			NP_001074000.1
	XM_006714289.3			XP_006714352.1
	XM_011532196.2			XP_011530498.1
	XM_011532197.2			XP_011530499.1
	XM_017008547.1			XP_016864036.1
	XM_017008548.1			XP_016864037.1
	XM_017008549.1			XP_016864038.1
	XM_017008550.1			XP_016864039.1
	XM_017008551.1			XP_016864040.1
	XM_017008552.1			XP_016864041.1
	XM_017008553.1			XP_016864042.1
	XM_017008554.1			XP_016864043.1
	XM_017008555.1			XP_016864044.1
	XM_017008556.1			XP_016864045.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv830105	Chr.4:145576238 - 145749385 on Build GRCh38	Loss	LOC285422 C4orf51 MMAA

More Information

Additional Information:

For this assay, SNP(s) [rs111814794] 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.

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation