Hs05455304_cn

• Gene Symbol: MAF
• Assay Reference Genome Location: Chr.16:79231424 on build GRCh38
• Cytoband: 16q23.2

Target Gene Details

• Entrez Gene ID: 4094
• Gene Name: MAF bZIP transcription factor
• Gene Aliases: AYGRP, CCA4, CTRCT21, c-MAF
• Location: Chr.16:79202624-79600725 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
MAF

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3639241	Chr.16:79219778 - 79258687 on Build GRCh38	Loss	MAF
esv2662766	Chr.16:79226224 - 79245902 on Build GRCh38	Deletion	MAF
nsv573287	Chr.16:79169293 - 79234387 on Build GRCh38	Loss	MAF LOC105371352 WWOX
esv3553726	Chr.16:79226104 - 79248315 on Build GRCh38	Deletion	MAF
esv3582366	Chr.16:79226608 - 79241358 on Build GRCh38	Loss	MAF
esv2762366	Chr.16:79226621 - 79241452 on Build GRCh38	Loss	MAF
nsv1063199	Chr.16:79224428 - 79248434 on Build GRCh38	Loss	MAF
esv2760426	Chr.16:79218610 - 79245768 on Build GRCh38	Gain	MAF
esv3639242	Chr.16:79224245 - 79245954 on Build GRCh38	Loss	MAF
nsv573285	Chr.16:79124285 - 80093429 on Build GRCh38	Gain	MAF LOC105371352 WWOX MAFTRR LINC01229

More Information

Additional Information:

For this assay, SNP(s) [rs116159645] 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, Non-exonic, DGV Variation