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Conclusions
• Mosaicism exists, but is overestimated by imperfect methods and lax criteria
• Intermediate copy number can originate from phenomena other than mosaicism
• Results from a single biopsy should not be considered a definitive diagnosis of mosaicism
Future Directions
• Make raw data available
• Publish more studies with rebiopsies of embryos classified as mosaic
• Perform systematic analysis of products of conception after transfer of “mosaic” embryos
• Develop time‐lapse integrated analysis (machine learning algorithms)
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