Assay Details
Target Gene Details
| Entrez Gene ID: | 101927174 | 
| Gene Name: | uncharacterized LOC101927174 | 
| Gene Aliases: | - | 
| Location: | Chr.3:112157-197407 on Build GRCh38 | 
| Assay Gene Location: | Within Intron 3 | 
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID | 
|---|---|---|---|---|
| LOC101927174 | XM_017007606.1 | XP_016863095.1 | 
Target Copy Number Variation Details
| DGV Version: | Release date: 2016-05-15, GRCh GRCh38 | 
| Target Variation | Location | CNV Subtype | Genes | 
|---|---|---|---|
| nsv1008449 | Chr.3:105120 - 189764 on Build GRCh38 | Gain |  LOC101927174 | 
| esv2759122 | Chr.3:29482 - 756820 on Build GRCh38 | Gain+Loss |  LOC101927174  CHL1-AS1  LINC01266  CHL1 | 
| esv3594872 | Chr.3:36658 - 319672 on Build GRCh38 | Loss |  LOC101927174  CHL1 | 
| dgv8142n54 | Chr.3:21733 - 143598 on Build GRCh38 | Loss |  LOC101927174  LOC102723448 | 
| esv2667629 | Chr.3:39576 - 1039187 on Build GRCh38 | Deletion |  LOC101927174  CHL1-AS1  LINC01266  CHL1  CNTN6 | 
| nsv428412 | Chr.3:29467 - 326726 on Build GRCh38 | Gain |  LOC101927174  CHL1 | 
| dgv8144n54 | Chr.3:72450 - 170062 on Build GRCh38 | Gain |  LOC101927174 | 
| nsv460301 | Chr.3:54290 - 132831 on Build GRCh38 | Gain |  LOC101927174 | 
| nsv524041 | Chr.3:53914 - 129625 on Build GRCh38 | Gain |  LOC101927174 | 
| nsv1009220 | Chr.3:44522 - 182907 on Build GRCh38 | Gain |  LOC101927174 | 
| dgv4605n100 | Chr.3:18655 - 115870 on Build GRCh38 | Gain |  LOC101927174  LOC102723448 | 
| esv3893585 | Chr.3:44574 - 267680 on Build GRCh38 | Gain |  LOC101927174  CHL1 | 
| esv3575523 | Chr.3:20214 - 160705 on Build GRCh38 | Gain |  LOC101927174  LOC102723448 | 
| esv3594879 | Chr.3:65856 - 151558 on Build GRCh38 | Gain |  LOC101927174 | 
| dgv4613n100 | Chr.3:52474 - 1799230 on Build GRCh38 | Loss |  LOC101927174  CHL1-AS1  LINC01266  CHL1  CNTN6 | 
| nsv997732 | Chr.3:93308 - 148728 on Build GRCh38 | Gain |  LOC101927174 | 
| esv2752007 | Chr.3:25192 - 175961 on Build GRCh38 | Gain |  LOC101927174 | 
| nsv998580 | Chr.3:111816 - 138468 on Build GRCh38 | Loss |  LOC101927174 | 
| nsv589242 | Chr.3:47730 - 388999 on Build GRCh38 | Gain |  LOC101927174  CHL1-AS1  CHL1 | 
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Additional Information:
				    	 
					    	
					        	
					            	For this assay, SNP(s) [rs112477063,rs115411117] 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 | 
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 Genomic Map
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