1p36 Deletion/Duplication Leave a Comment / Uncategorized / By claritasgenomics Skip to main content Search form Search Search Menu The Claritas Experience Tests & Ordering Complete Test Menu How to Order Order Specimen Collection Kits Sample Requirements Data Return Program What We Do Resources Clinicians Clinical Experience Orthogonal Approach Expert Network NextCODE Services Overview Clinical Resources and Services Billing and Financial Assistance Data Return Program Families Family Experience About the Test Share Your Data Resources and Services Billing and Financial Assistance Researchers Research Experience Data Return Program Research Opportunities NextCODE Services Overview About Us Claritas Story Leadership Partnerships News and Events Careers Resources Certifications and Licenses Help Center Order Test 1p36 Deletion/Duplication Home 1p36 Deletion/Duplication Test Background 1p36 deletion is characterized by typical craniofacial features, developmental delay/intellectual disability, and hypotonia. MLPA detects greater than 95% of cases. Lab Method MLPA Scroll
