Hs03956110_cn

• Gene Symbol: LOC105371932
• Assay Reference Genome Location: Chr.17:35242428 on build GRCh38
• Cytoband: 17q12

Target Gene Details

• Entrez Gene ID: 105371932
• Gene Name: uncharacterized LOC105371932
• Gene Aliases: -
• Location: Chr.17:35240043-35247472 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC105371932	XM_017025492.1			XP_016880981.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2422399	Chr.17:35212221 - 35291582 on Build GRCh38	Deletion	SLFN5 LOC105371932
esv3892998	Chr.17:35106468 - 35295755 on Build GRCh38	Loss	FNDC8 UNC45B SLC35G3 NLE1 RAD51D RAD51L3-RFFL SLFN5 LOC105371932
nsv574741	Chr.17:35225256 - 35500115 on Build GRCh38	Loss	SLFN12L SLFN11 SLFN5 LOC105371933 LOC105371932 SLFN12 SLFN13

More Information

Additional Information:

For this assay, SNP(s) [rs114664206] 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