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aCGH Deletion/Duplication Analysis

Order Code: 4800

Also Known as

ACTN1, ADAMTS13, BLOC1S3, BLOC1S6, C3, C4BPA, C4BPB, CD46, CFB, CFI, CYCS, DGKE, ELANE, F10, F11, F13A1, F2, F5, F7, F8, F9, Factor 8, Factor 9, Factor IX, Factor VIII, FGA, FGB, FGG, G6PC3, GATA1, GGCX, GP1BA, GP1BB, GP6, GP9, HAX1, Hemophilia, Hemophilia A, Hemophilia B, HOXA11, HPS1, HPS3, HPS4, HPS5, HPS6, HRG, LMAN1, LMNA, MPL, MYH9, PLA2G4A, PLAU, PROC, RBM8A, RUNX1, SERPINC1, STXBP2, TBXA2R, THBD, VKORC1, Von Willebrand Disease, Von Willebrand Factor, VWD, VWF, WAS

Test Information

This custom designed, high density gene-foused array allows for the detection of small deletions and duplications within a single exon of a given gene, and large deletions and duplications encompassing one or more exons, or the entire gene.

Sample Requirements

Fetal: Amniotic Fluid, CVS, Cultured Amniocytes or Cultured CVS; Parental/Patient: EDTA Whole Blood (lavender top)

Additional Sample Requirements

If sending DNA, client must send >1µg of DNA at >50ng/µl.

Shipping Information

Room Temperature

Requested Volume

Fetal: 7-15 ml Amniotic Fluid or 5-10 mg CVS, backup culture of Amniocytes or CVS is highly recommended; Two T25 flasks Cultured Amniocytes or CVS (2x10^6 minimum); Parental/Patient: 3-5 ml

Minimum/Pediatric Volume

Fetal: Call Laboratory; Parental/Patient: 2 ml

CPT Codes

F8: 81406 and all other genes use: 81479

Method

array Comparative Genomic Hybridization

Turnaround Time

21 days

DEX Z-Code™

Yes, visit app.dexzcodes.com

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