Hs05052302_cn

• Gene Symbol: FAM110B
• Assay Reference Genome Location: Chr.8:57994509 on build GRCh38
• Cytoband: 8q12.1

Target Gene Details

• Entrez Gene ID: 90362
• Gene Name: family with sequence similarity 110 member B
• Gene Aliases: C8orf72
• Location: Chr.8:57994444-58149718 on Build GRCh38
• Assay Gene Location: Within Exon 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM110B	XM_005251324.2	1	66	XP_005251381.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1075139	Chr.8:57994140 - 57994641 on Build GRCh38	Deletion	FAM110B
nsv1119181	Chr.8:57994041 - 57994641 on Build GRCh38	Deletion	FAM110B
nsv831324	Chr.8:57931592 - 58132750 on Build GRCh38	Loss	FAM110B LINC01602

More Information

Additional Information:

For this assay, SNP(s) [rs151294209] 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, Exonic, DGV Variation