Optical genome mapping reveals balanced and unbalanced genetic changes associated with tumor‐forming potential in an early‐stage prostate cancer epithelial subline (M2205) von Paulraj, Prabakaran, Barrie, Elizabeth, Jackson‐Cook, Colleen

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Acute megakaryoblastic leukemia with trisomy 3 and CBFA2T3::GLIS2: A case report von Gillam, Joseph, Catic, Aida, Paulraj, Prabakaran, Dalton, Justin, Lai, Guanhua, Jackson‐Cook, Colleen, Turner, Scott, Ferreira‐Gonzalez, Andrea, Barrie, Elizabeth

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Pediatric acute myeloid leukemia with t(7;21)(p22;q22) von Paulraj, Prabakaran, Diamond, Steven, Razzaqi, Faisal, Ozeran, J. Daniel, Longhurst, Maria, Andersen, Erica F., Toydemir, Reha M., Hong, Bo

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Optical genomic mapping reveals balanced and unbalanced cytogenetic findings associated with tumor-forming potential in a prostate cancer cell line (M2205) von Paulraj, Prabakaran, Barrie, Elizabeth S., Jackson-Cook, Colleen

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A rare 2p11.2 microdeletion in an infant with T cell lymphopenia and an abnormal newborn screen for severe combined immunodeficiency von Rafferty, Kelly, Barrie, Elizabeth S., Jackson-Cook, Colleen, Paulraj, Prabakaran

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eP388 - Optical genomic mapping reveals balanced and unbalanced cytogenetic findings associated with tumor-forming potential in a prostate cancer cell line (M2205) von Paulraj, Prabakaran, Barrie, Elizabeth S., Jackson-Cook, Colleen

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eP375 - A rare 2p11.2 microdeletion in an infant with T cell lymphopenia and an abnormal newborn screen for severe combined immunodeficiency von Rafferty, Kelly, Barrie, Elizabeth S., Jackson-Cook, Colleen, Paulraj, Prabakaran

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Trisomy 3 and CBFA2T3-GLIS2 fusion in a child with acute megakaryoblastic leukemia without Down syndrome von Catic, Aida, Barrie, Elizabeth S., Turner, Scott, Ferreira-Gonzalez, Andrea, Jackson-Cook, Colleen, Lai, Guanhua, Dalton, Justin, Paulraj, Prabakaran

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eP066 - Trisomy 3 and CBFA2T3-GLIS2 fusion in a child with acute megakaryoblastic leukemia without Down syndrome von Catic, Aida, Barrie, Elizabeth S., Turner, Scott, Ferreira-Gonzalez, Andrea, Jackson-Cook, Colleen, Lai, Guanhua, Dalton, Justin, Paulraj, Prabakaran

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Identification of Parental Chromosomes Involved in Translocations BCR-ABL, t(9;22) and PML-RARA, t(15;17) von CHAUDHURI, Jyoti P, KARAMANOV, Sultan, PAULRAJ, Prabakaran, MCGILL, John R, WALTHER, Joachim-U

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eP443 - Standardizing the classification of recurrent copy number variants–incorporation of sub-clinical phenotype data for CNVs with reduced penetrance von Herriges, John, Andersen, Erica, Coe, Bradley, Conlin, Laura, Hilton, Benjamin, Jobanputra, Vaidehi, Levy, Brynn, Paulraj, Prabakaran, Runke, Cassandra, Schleede, Justin, Zhang, Shulin, Martin, Christa

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Standardizing the classification of recurrent copy number variants–incorporation of sub-clinical phenotype data for CNVs with reduced penetrance von Herriges, John, Andersen, Erica, Coe, Bradley, Conlin, Laura, Hilton, Benjamin, Jobanputra, Vaidehi, Levy, Brynn, Paulraj, Prabakaran, Runke, Cassandra, Schleede, Justin, Zhang, Shulin, Martin, Christa

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Severe Graft-Versus-Host Disease Following Solid-Organ Transplant Confirmed by Chimerism Studies and Cytogenetic Analyses von Rafferty, Kelly A., Barrie, Elizabeth S., Turner, Scott A., Ferreira-Gonzalez, Andrea, Jackson-Cook, Colleen, Paulraj, Prabakaran

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A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay von Paulraj, Prabakaran, Bosworth, Michelle, Longhurst, Maria, Hornbuckle, Callie, Gotway, Garrett, Lamb, Allen N., Andersen, Erica F.

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Multiple Congenital Anomalies and Global Developmental Delay in a Patient with Interstitial 6q25.2q26 Deletion: A Diagnostic Odyssey von Paulraj, Prabakaran, Palumbos, Janice C., Openshaw, Amanda, Carey, John C., Toydemir, Reha M.

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Chronic myelomonocytic leukemia with ETV6-ABL1 rearrangement and SMC1A mutation von Cessna, Melissa H., Paulraj, Prabakaran, Hilton, Benjamin, Sadre-Bazzaz, Kianoush, Szankasi, Philippe, Cluff, Alice, Patel, Jay L., Hoda, Daanish, Toydemir, Reha M.

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3. Standardizing recurrent copy number variant classification – From benign to reduced and high penetrance regions von Andersen, Erica F., Herriges, John, Coe, Bradley, Conlin, Laura, Goodenberger, McKinsey, Hilton, Benjamin, Jobanputra, Vaidehi, Levy, Brynn, Paulraj, Prabakaran, Riggs, Erin Rooney, Runke, Cassandra, Schleede, Justin, Speevak, Marsha, Zhang, Shulin, Thorland, Erik, Martin, Christa Lese

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44. Ring chromosome 7 in patients with dysplastic features in bone marrow von Paulraj, Prabakaran, Tantravahi, Srinivas, Reddy, Anurag, Longhurst, Maria C., Andersen, Erica F., Prchal, Josef, Toydemir, Reha M., Hong, Bo

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28. Dosage sensitivity curation of recurrent copy number variant regions von Andersen, Erica, Burnside, Rachel, Coe, Bradley, Conlin, Laura, Herriges, John, Higginbotham, Ted, Hilton, Benjamin, Jobanputra, Vaidehi, Kearney, Hutton, Ouyang, Karen, Paulraj, Prabakaran, Riggs, Erin Rooney, Rowsey, Ross, Speevak, Marsha, Thorland, Erik, Zhang, Lei, Martin, Christa Lese

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Multiple Congenital Anomalies and Global Developmental Delay in a Patient with Interstitial 6q25.2q26 Deletion: A Diagnostic Odyssey von Paulraj, Prabakaran, Palumbos, Janice C, Openshaw, Amanda, Carey, John C, Toydemir, Reha M

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